ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. Most common adverse reactions are cluster of symptoms called cinchonism, which occurs to some degree in almost all patients taking quinine: headache, vasodilation and sweating, nausea, tinnitus, hearing impairment, vertigo or dizziness, blurred vision, disturbance in color perception, vomiting, diarrhea, abdominal pain, deafness, blindness, and disturbances in cardiac rhythm or conduction (6.1). To report SUSPECTED ADVERSE REACTIONS, contact Mutual Pharmaceutical Company, Inc. at 1-888-351-3786 or drugsafetyurlpharma.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Overall. Quinine can adversely affect almost every body system. The most common adverse events associated with quinine use are cluster of symptoms called cinchonism, which occurs to some degree in almost all patients taking quinine. Symptoms of mild cinchonism include headache, vasodilation and sweating, nausea, tinnitus, hearing impairment, vertigo or dizziness, blurred vision, and disturbance in color perception. More severe symptoms of cinchonism are vomiting, diarrhea, abdominal pain, deafness, blindness, and disturbances in cardiac rhythm or conduction. Most symptoms of cinchonism are reversible and resolve with discontinuation of quinine.The following ADVERSE REACTIONS have been reported with quinine sulfate. Most of these reactions are thought to be uncommon, but the actual incidence is unknown:General: fever, chills, sweating, flushing, asthenia, lupus-like syndrome, and hypersensitivity reactions.Hematologic: agranulocytosis, hypoprothrombinemia, thrombocytopenia, disseminated intravascular coagulation, hemolytic anemia; hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, idiopathic thrombocytopenic purpura, petechiae, ecchymosis, hemorrhage, coagulopathy, blackwater fever, leukopenia, neutropenia, pancytopenia, aplastic anemia, and lupus anticoagulant.Neuropsychiatric: headache, diplopia, confusion, altered mental status, seizures, coma, disorientation, tremors, restlessness, ataxia, acute dystonic reaction, aphasia, and suicide.Dermatologic: cutaneous rashes, including urticarial, papular, or scarlatinal rashes, pruritus, bullous dermatitis, exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, fixed drug eruption, photosensitivity reactions, allergic contact dermatitis, acral necrosis, and cutaneous vasculitis.Respiratory: asthma, dyspnea, pulmonary edema.Cardiovascular: chest pain, vasodilatation, hypotension, postural hypotension, tachycardia, bradycardia, palpitations, syncope, atrioventricular block, atrial fibrillation, irregular rhythm, unifocal premature ventricular contractions, nodal escape beats, waves, QT prolongation, ventricular fibrillation, ventricular tachycardia, torsades de pointes, and cardiac arrest.Gastrointestinal: nausea, vomiting, diarrhea, abdominal pain, gastric irritation, and esophagitis.Hepatobiliary: granulomatous hepatitis, hepatitis, jaundice, and abnormal liver function tests.Metabolic: hypoglycemia and anorexia.Musculoskeletal: myalgias and muscle weakness. Renal: hemoglobinuria, renal failure, renal impairment, and acute interstitial nephritis.Special Senses: visual disturbances, including blurred vision with scotomata, sudden loss of vision, photophobia, diplopia, night blindness, diminished visual fields, fixed pupillary dilatation, disturbed color vision, optic neuritis, blindness, vertigo, tinnitus, hearing impairment, and deafness.

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. Quinine is an antimalarial agent [see Clinical Pharmacology (12.4) ].. 12.2 Pharmacodynamics. QTc interval prolongation was studied in double-blind, multiple dose, placebo- and positive-controlled crossover study in young (N=13, 20 to 39 years) and elderly (N=13, 65 to 78 years) subjects. After days of dosing with QUALAQUIN 648 mg three times daily, the maximum mean (95% upper confidence bound) differences in QTcI from placebo after baseline correction was 27.7 (32.2) ms.Prolongation of the PR and QRS interval was also noted in subjects receiving QUALAQUIN. The maximum mean (95% upper confidence bound) difference in PR from placebo after baseline-correction was 14.5 (18.0) ms. The maximum mean (95% upper confidence bound) difference in QRS from placebo after baseline-correction was 11.5 (13.3) ms. [see Warnings and Precautions (5.3) ].. 12.3 Pharmacokinetics. AbsorptionThe oral bioavailability of quinine is 76 to 88% in healthy adults. Quinine exposure is higher in patients with malaria than in healthy subjects. After single oral dose of quinine sulfate, the mean quinine Tmax was longer, and mean AUC and Cmax were higher in patients with uncomplicated P. falciparum malaria than in healthy subjects, as shown in Table below.TABLE Pharmacokinetic Parameters of Quinine in Healthy Subjects and Patients with Uncomplicated P. falciparum Malaria after Single Dose of Oral Quinine Sulfate CapsulesHealthy Subjects(N 23)Mean +- SDUncomplicated P. falciparum Malaria Patients(N 15)Mean +- SDDose (mg/kg)Quinine Sulfate dose was 648 mg (approximately 8.7 mg/kg) in healthy subjects; and 10 mg/kg in patients with malaria 8.710Tmax (h)2.8 +- 0.85.9 +- 4.7Cmax (mcg/mL)3.2 +- 0.78.4AUC0-12 (mcgh/mL)28.073.0QUALAQUIN capsules may be administered without regard to meals. When single oral 324 mg capsule of QUALAQUIN was administered to healthy subjects (N=26) with standardized high-fat breakfast, the mean Tmax of quinine was prolonged to about 4.0 hours, but the mean Cmax and AUC0-24h were similar to those achieved when QUALAQUIN capsule was given under fasted conditions [see Dosage and Administration (2.1) ].. DistributionIn patients with malaria, the volume of distribution (Vd/F) decreases in proportion to the severity of the infection. In published studies with healthy subjects who received single oral 600 mg dose of quinine sulfate, the mean Vd/F ranged from 2.5 to 7.1 L/kg.Quinine is moderately protein-bound in blood in healthy subjects, ranging from 69 to 92%. During active malarial infection, protein binding of quinine is increased to 78 to 95%, corresponding to the increase in 1-acid glycoprotein that occurs with malaria infection.Intra-erythrocytic levels of quinine are approximately 30 to 50% of the plasma concentration.Quinine penetrates relatively poorly into the cerebrospinal fluid (CSF) in patients with cerebral malaria, with CSF concentration approximately to 7% of plasma concentration.In one study, quinine concentrations in placental cord blood and breast milk were approximately 32% and 31%, respectively, of quinine concentrations in maternal plasma. The estimated total dose of quinine secreted into breast milk was less than to mg per day [see Use in Specific Populations (8.1, 8.3) ].. MetabolismQuinine is metabolized almost exclusively via hepatic oxidative cytochrome P450 (CYP) pathways, resulting in four primary metabolites, 3-hydroxyquinine, 2-quinone, O-desmethylquinine, and 10,11-dihydroxydihydroquinine. Six secondary metabolites result from further biotransformation of the primary metabolites. The major metabolite, 3-hydroxyquinine, is less active than the parent drug.In vitro studies using human liver microsomes and recombinant P450 enzymes have shown that quinine is metabolized mainly by CYP3A4. Depending on the in vitro experimental conditions, other enzymes, including CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP2E1 were shown to have some role in the metabolism of quinine.. Elimination/ExcretionQuinine is eliminated primarily via hepatic biotransformation. Approximately 20% of quinine is excreted unchanged in urine. Because quinine is reabsorbed when the urine is alkaline, renal excretion of the drug is twice as rapid when the urine is acidic than when it is alkaline.In various published studies, healthy subjects who received single oral 600 mg dose of quinine sulfate exhibited mean plasma clearance ranging from 0.08 to 0.47 L/h/kg (median value: 0.17 L/h/kg) with mean plasma elimination half-life of 9.7 to 12.5 hours.In 15 patients with uncomplicated malaria who received 10 mg/kg oral dose of quinine sulfate, the mean total clearance of quinine was slower (approximately 0.09 L/h/kg) during the acute phase of the infection, and faster (approximately 0.16 L/h/kg) during the recovery or convalescent phase.. Extracorporeal Elimination: Administration of multiple-dose activated charcoal (50 grams administered hours after quinine dosing followed by further doses over the next 12 hours) decreased the mean quinine elimination half-life from 8.2 to 4.6 hours, and increased the mean quinine clearance by 56% (from 11.8 L/h to 18.4 L/h) in healthy adult subjects who received single oral 600 mg dose of quinine sulfate. Likewise, in symptomatic patients with acute quinine poisoning who received multiple-dose activated charcoal (50 grams every hours), the mean quinine elimination half-life was shortened to 8.1 hours in comparison to half-life of approximately 26 hours in patients who did not receive activated charcoal [see Overdosage (10) ].In patients with quinine poisoning, forced acid diuresis did not change the half-life of quinine elimination (25.1 +- 4.6 hours vs. 26.5 +- 5.8 hours), or the amount of unchanged quinine recovered in the urine, in comparison to patients not treated in this manner [see Overdosage (10) ].. Specific Populations. Pediatric Patients: The pharmacokinetics of quinine in children (1.5 to 12 years old) with uncomplicated P. falciparum malaria appear to be similar to that seen in adults with uncomplicated malaria. Furthermore, as seen in adults, the mean total clearance and the volume of distribution of quinine were reduced in pediatric patients with malaria as compared to the healthy pediatric controls. Table below provides comparison of the mean +- SD pharmacokinetic parameters of quinine in pediatric patients vs. healthy pediatric controls.TABLE Quinine Pharmacokinetic Parameters Following the First 10 mg/kg Quinine Sulfate Oral Dose in Healthy Pediatric Controls and Pediatric Patients with Acute Uncomplicated P. falciparum MalariaHealthy Pediatric Controlsage 1.5 to 12 years (N 5)Mean +- SDP. falciparum Malaria Pediatric Patients(N 15)Mean +- SDTmax (h)2.04.0Cmax (mcg/mL)3.4 +- 1.187.5 +- 1.1Half-life (h)3.2 +- 0.312.1 +- 1.4Total CL (L/h/kg)0.30 +- 0.040.06 +- 0.01Vd (L/kg)1.43 +- 0.180.87 +- 0.12. Geriatric Patients: Following single oral dose of 600 mg quinine sulfate, the mean AUC was about 38% higher in healthy elderly subjects (65 to 78 years old) than in 12 younger subjects (20 to 35 years old). The mean Tmax and Cmax were similar in elderly and younger subjects after single oral dose of quinine sulfate 600 mg. The mean oral clearance of quinine was significantly decreased, and the mean elimination half-life was significantly increased in elderly subjects compared with younger subjects (0.06 vs. 0.08 L/h/kg, and 18.4 hours vs. 10.5 hours, respectively). Although there was no significant difference in the renal clearance of quinine between the two age groups, elderly subjects excreted larger proportion of the dose in urine as unchanged drug than younger subjects (16.6% vs. 11.2%).After single 648 mg dose or at steady state, following quinine sulfate 648 mg given three times daily for days, no difference in the rate and extent of absorption or clearance of quinine was seen between 13 elderly subjects (65 to 78 years old) and 14 young subjects (20 to 39 years old). The mean elimination half-life was 20% longer in the elderly subjects (24.0 hours) than in younger subjects (20.0 hours). The steady state Cmax (+-SD) and AUC0-8 (+-SD) for healthy volunteers are 6.8 +- 1.24 mcg/mL and 48.8 +- 9.15 mcgh/mL, respectively, following days of oral quinine sulfate 648 mg three times daily. The steady state pharmacokinetic parameters in healthy elderly subjects were similar to the pharmacokinetic parameters in healthy young subjects.. Renal Impairment: Following single oral 600 mg dose of quinine sulfate in otherwise healthy subjects with severe chronic renal failure not receiving any form of dialysis (mean serum creatinine 9.6 mg/dL), the median AUC was higher by 195% and the median Cmax was higher by 79% than in subjects with normal renal function (mean serum creatinine 1 mg/dL). The mean plasma half-life in subjects with severe chronic renal impairment was prolonged to 26 hours compared to 9.7 hours in the healthy controls. Computer assisted modeling and simulation indicates that in patients with malaria and severe chronic renal failure, dosage regimen consisting of one loading dose of 648 mg QUALAQUIN followed 12 hours later by maintenance dosing regimen of 324 mg every 12 hours will provide adequate systemic exposure to quinine [see Dosage and Administration (2.2) ]. The effects of mild and moderate renal impairment on the pharmacokinetics and safety of quinine sulfate are not known.Negligible to minimal amounts of circulating quinine in the blood are removed by hemodialysis or hemofiltration. In subjects with chronic renal failure (CRF) on hemodialysis, only about 6.5% of quinine is removed in hour. Plasma quinine concentrations do not change during or shortly after hemofiltration in subjects with CRF [see Overdosage (10) ].. Hepatic Impairment: In otherwise healthy subjects with mild hepatic impairment (Child-Pugh A; N=10), who received single 500 mg dose of quinine sulfate, there was no significant difference in quinine pharmacokinetic parameters or exposure to the primary metabolite, 3-hydroxyquinine as compared to healthy controls (N=10). In otherwise healthy subjects with moderate hepatic impairment (Child-Pugh B; N=9) who received single oral 600 mg dose of quinine sulfate, the mean AUC increased by 55% without significant change in mean Cmax, as compared to healthy volunteer controls (N=6). In subjects with hepatitis, the absorption of quinine was prolonged, the elimination half-life was increased, the apparent volume of distribution was higher, but there was no significant difference in weight-adjusted clearance. Therefore, in patients with mild to moderate hepatic impairment, dosage adjustment is not needed, but patients should be monitored closely for adverse effects of quinine [see Use in Specific Populations (8.7) ].In subjects with severe hepatic impairment (Child-Pugh C; N=10), quinine oral clearance (CL/F) was reduced as was formation of the primary 3-hydroxyquinine metabolite. Volume of distribution (Vd/F) was higher and the plasma elimination half-life was increased. Therefore, quinine is not indicated in this population and alternate therapy should be administered [see Dosage and Administration (2.3) ].. 12.4 Microbiology. Mechanism of ActionQuinine inhibits nucleic acid synthesis, protein synthesis, and glycolysis in Plasmodium falciparum and can bind with hemazoin in parasitized erythrocytes. However, the precise mechanism of the antimalarial activity of quinine sulfate is not completely understood.. Activity In Vitro and In Vivo Quinine sulfate acts primarily on the blood schizont form of P. falciparum. It is not gametocidal and has little effect on the sporozoite or pre-erythrocytic forms.. Drug ResistanceStrains of P. falciparum with decreased susceptibility to quinine can be selected in vivo. P. falciparum malaria that is clinically resistant to quinine has been reported in some areas of South America, Southeast Asia, and Bangladesh.

CONTRAINDICATIONS SECTION.

4 CONTRAINDICATIONS. QUALAQUIN is contraindicated in patients with the following: Prolonged QT interval. One case of fatal ventricular arrhythmia was reported in an elderly patient with prolonged QT interval at baseline, who received quinine sulfate intravenously for P. falciparum malaria [see Warnings and Precautions (5.3) ]. Glucose-6-phosphate dehydrogenase (G6PD) deficiency. Hemolysis can occur in patients with G6PD deficiency receiving quinine. Known hypersensitivity reactions to quinine.These include, but are not limited to, the following [see Warnings and Precautions (5.6) ]:ThrombocytopeniaIdiopathic thrombocytopenia purpura (ITP) and Thrombotic thrombocytopenic purpura (TTP)Hemolytic uremic syndrome (HUS)Blackwater fever (acute intravascular hemolysis, hemoglobinuria, and hemoglobinemia) Known hypersensitivity to mefloquine or quinidine: cross-sensitivity to quinine has been documented [see Warnings and Precautions (5.6) ]. Myasthenia gravis. Quinine has neuromuscular blocking activity, and may exacerbate muscle weakness.Optic neuritis. Quinine may exacerbate active optic neuritis [see Adverse Reactions (6) ]. Prolonged QT interval. One case of fatal ventricular arrhythmia was reported in an elderly patient with prolonged QT interval at baseline, who received quinine sulfate intravenously for P. falciparum malaria [see Warnings and Precautions (5.3) ]. Glucose-6-phosphate dehydrogenase (G6PD) deficiency.. Hemolysis can occur in patients with G6PD deficiency receiving quinine.. Known hypersensitivity reactions to quinine.These include, but are not limited to, the following [see Warnings and Precautions (5.6) ]:ThrombocytopeniaIdiopathic thrombocytopenia purpura (ITP) and Thrombotic thrombocytopenic purpura (TTP)Hemolytic uremic syndrome (HUS)Blackwater fever (acute intravascular hemolysis, hemoglobinuria, and hemoglobinemia) These include, but are not limited to, the following [see Warnings and Precautions (5.6) ]:ThrombocytopeniaIdiopathic thrombocytopenia purpura (ITP) and Thrombotic thrombocytopenic purpura (TTP)Hemolytic uremic syndrome (HUS)Blackwater fever (acute intravascular hemolysis, hemoglobinuria, and hemoglobinemia) Thrombocytopenia. Idiopathic thrombocytopenia purpura (ITP) and Thrombotic thrombocytopenic purpura (TTP). Hemolytic uremic syndrome (HUS). Blackwater fever (acute intravascular hemolysis, hemoglobinuria, and hemoglobinemia) Known hypersensitivity to mefloquine or quinidine: cross-sensitivity to quinine has been documented [see Warnings and Precautions (5.6) ]. Myasthenia gravis. Quinine has neuromuscular blocking activity, and may exacerbate muscle weakness.Optic neuritis. Quinine may exacerbate active optic neuritis [see Adverse Reactions (6) ]. Myasthenia gravis. Quinine has neuromuscular blocking activity, and may exacerbate muscle weakness.. Optic neuritis. Quinine may exacerbate active optic neuritis [see Adverse Reactions (6) ].. QUALAQUIN is contraindicated in patients with the following:Prolongation of QT interval (4)Glucose-6-phosphate dehydrogenase (G6PD) deficiency (4)Myasthenia gravis (4)Known hypersensitivity to quinine, mefloquine, or quinidine (4)Optic neuritis (4). Prolongation of QT interval (4). Glucose-6-phosphate dehydrogenase (G6PD) deficiency (4). Myasthenia gravis (4). Known hypersensitivity to quinine, mefloquine, or quinidine (4). Optic neuritis (4).

DRUG INTERACTIONS SECTION.

7 DRUG INTERACTIONS. Interacting DrugInteractionDrugs known to prolong QT interval (e.g., Class IA and Class III antiarrhythmic agents).QUALAQUIN prolongs QT interval, ECG abnormalities including QT prolongation and Torsades de Pointes. Avoid concomitant use (5.3).Other antimalarials (e.g., halofantrine, mefloquine).ECG abnormalities including QT prolongation. Avoid concomitant use (5.3, 7.2).CYP3A4 inducers or inhibitorsAlteration in plasma quinine concentration. Monitor for lack of efficacy or increased adverse events of quinine (7.1).CYP3A4 and CYP2D6 substratesQuinine is an inhibitor of CYP3A4 and CYP2D6. Monitor for lack of efficacy or increased adverse events of the co-administered drug (7.2).DigoxinIncreased digoxin plasma concentration (5.8, 7.1).See full prescribing information for complete list of reported and potential interactions.. 7.1 Effects of Drugs and Other Substances on Quinine Pharmacokinetics. Quinine is P-gp substrate and is primarily metabolized by CYP3A4. Other enzymes, including CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP2E1 may contribute to the metabolism of quinine [see Clinical Pharmacology (12.3) ].. Antacids: Antacids containing aluminum and/or magnesium may delay or decrease absorption of quinine. Concomitant administration of these antacids with QUALAQUIN should be avoided.. Antiepileptics (AEDs) (carbamazepine, phenobarbital, and phenytoin): Carbamazepine, phenobarbital, and phenytoin are CYP3A4 inducers and may decrease quinine plasma concentrations if used concurrently with QUALAQUIN.. Cholestyramine: In healthy subjects who received quinine sulfate 600 mg with or without grams of cholestyramine resin, no significant difference in quinine pharmacokinetic parameters was seen.. Cigarette Smoking (CYP1A2 inducer): In healthy male heavy smokers, the mean quinine AUC following single 600 mg dose was 44% lower, the mean Cmax was 18% lower, and the elimination half-life was shorter (7.5 hours versus 12 hours) than in their non-smoking counterparts. However, in malaria patients who received the full 7-day course of quinine therapy, cigarette smoking produced only 25% decrease in median quinine AUC and 16.5% decrease in median Cmax, suggesting that the already reduced clearance of quinine in acute malaria could have diminished the metabolic induction effect of smoking. Because smoking did not appear to influence the therapeutic outcome in malaria patients, it is not necessary to increase the dose of quinine in the treatment of acute malaria in heavy cigarette smokers.. Grapefruit juice (P-gp/CYP3A4 inhibitor): In pharmacokinetic study involving 10 healthy subjects, the administration of single 600 mg dose of quinine sulfate with grapefruit juice (full-strength or half-strength) did not significantly alter the pharmacokinetic parameters of quinine. QUALAQUIN may be taken with grapefruit juice.. Histamine H2-receptor blockers [cimetidine, ranitidine (nonspecific CYP450 inhibitors)]: In healthy subjects who were given single oral 600 mg dose of quinine sulfate after pretreatment with cimetidine (200 mg three times daily and 400 mg at bedtime for days) or ranitidine (150 mg twice daily for days), the apparent oral clearance of quinine decreased and the mean elimination half-life increased significantly when given with cimetidine but not with ranitidine. Compared to untreated controls, the mean AUC of quinine increased by 20% with ranitidine and by 42% with cimetidine (p<0.05) without significant change in mean quinine Cmax. When quinine is to be given concomitantly with histamine H2-receptor blocker, the use of ranitidine is preferred over cimetidine. Although cimetidine and ranitidine may be used concomitantly with QUALAQUIN, patients should be monitored closely for adverse events associated with quinine.. Isoniazid: Isoniazid 300 mg/day pretreatment for week did not significantly alter the pharmacokinetic parameter values of quinine. Adjustment of QUALAQUIN dosage is not necessary when isoniazid is given concomitantly.. Ketoconazole (CYP3A4 inhibitor): In crossover study, healthy subjects (N=9) who received single oral dose of quinine hydrochloride (500 mg) concomitantly with ketoconazole (100 mg twice daily for days) had mean quinine AUC that was higher by 45% and mean oral clearance of quinine that was 31% lower than after receiving quinine alone. Although no change in the QUALAQUIN dosage regimen is necessary with concomitant ketoconazole, patients should be monitored closely for adverse reactions associated with quinine.. Macrolide antibiotics (erythromycin, troleandomycin) (CYP3A4 inhibitors): In crossover study (N=10), healthy subjects who received single oral 600 mg dose of quinine sulfate with the macrolide antibiotic, troleandomycin (500 mg every hours) exhibited 87% higher mean quinine AUC, 45% lower mean oral clearance of quinine, and 81% lower formation clearance of the main metabolite, 3-hydroxyquinine, than when quinine was given alone.Erythromycin was shown to inhibit the in vitro metabolism of quinine in human liver microsomes, an observation confirmed by an in vivo interaction study. In crossover study (N=10), healthy subjects who received single oral 500 mg dose of quinine sulfate with erythromycin (600 mg every hours for four days) showed decrease in quinine oral clearance (CL/F), an increase in half-life, and decreased metabolite (3-hydroxyquinine) to quinine AUC ratio, as compared to when quinine was given with placebo.Therefore, concomitant administration of macrolide antibiotics such as erythromycin or troleandomycin with QUALAQUIN should be avoided [see Warnings and Precautions (5.3) ].. Oral contraceptives (estrogen, progestin): In healthy females who were using single-ingredient progestin or combination estrogen-containing oral contraceptives, the pharmacokinetic parameters of single 600 mg dose of quinine sulfate were not altered in comparison to those observed in age-matched female control subjects not using oral contraceptives.. Rifampin (CYP3A4 inducer): In patients with uncomplicated P. falciparum malaria who received quinine sulfate 10 mg/kg concomitantly with rifampin 15 mg/kg/day for days (N=29), the median AUC of quinine between days and of therapy was 75% lower as compared to those who received quinine monotherapy. In healthy subjects (N=9) who received single oral 600 mg dose of quinine sulfate after weeks of pretreatment with rifampin 600 mg/day, the mean quinine AUC and Cmax decreased by 85% and 55%, respectively. Therefore, the concomitant administration of rifampin with QUALAQUIN should be avoided [see Warnings and Precautions (5.4) ].. Ritonavir: In healthy subjects who received single oral 600 mg dose of quinine sulfate with the 15th dose of ritonavir (200 mg every 12 hours for days), there were 4-fold increases in the mean quinine AUC and Cmax, and an increase in the mean elimination half-life (13.4 hours versus 11.2 hours), compared to when quinine was given alone. Therefore, the concomitant administration of ritonavir with QUALAQUIN capsules should be avoided [see also Drug Interactions (7.2) ].. Tetracycline: In patients with acute uncomplicated P. falciparum malaria who were treated with oral quinine sulfate (600 mg every hours for days) in combination with oral tetracycline (250 mg every hours for days), the mean plasma quinine concentrations were about two-fold higher than in patients who received quinine monotherapy. Although tetracycline may be concomitantly administered with QUALAQUIN, patients should be monitored closely for adverse reactions associated with quinine sulfate.. Theophylline or aminophylline: In 20 healthy subjects who received multiple doses of QUALAQUIN (648 mg every hours 7 days) with single 300 mg oral dose of theophylline, the quinine mean Cmax and AUC were increased by 13% and 14% respectively. Although no change in the QUALAQUIN dosage regimen is necessary with concomitant theophylline or aminophylline, patients should be monitored closely for adverse reactions associated with quinine.. Urinary alkalizers (acetazolamide, sodium bicarbonate): Urinary alkalinizing agents may increase plasma quinine concentrations.. 7.2 Effects of Quinine on the Pharmacokinetics of Other Drugs. Results of in vivo drug interaction studies suggest that quinine has the potential to inhibit the metabolism of drugs that are substrates of CYP3A4 and CYP2D6. Quinine inhibits P-gp and has the potential to affect the transport of drugs that are P-gp substrates.. Anticonvulsants (carbamazepine, phenobarbital, and phenytoin): single 600 mg oral dose of quinine sulfate increased the mean plasma Cmax, and AUC0-24 of single oral doses of carbamazepine (200 mg) and phenobarbital (120 mg) but not phenytoin (200 mg) in healthy subjects. The mean AUC increases of carbamazepine, phenobarbital and phenytoin were 104%, 81% and 4%, respectively; the mean increases in Cmax were 56%, 53%, and 4%, respectively. Mean urinary recoveries of the three antiepileptics over 24 hours were also profoundly increased by quinine. If concomitant administration with carbamazepine or phenobarbital cannot be avoided, frequent monitoring of anticonvulsant drug concentrations is recommended. Additionally, patients should be monitored closely for adverse reactions associated with these anticonvulsants.. Astemizole (CYP3A4 substrate): Elevated plasma astemizole concentrations were reported in subject who experienced torsades de pointes after receiving three doses of quinine sulfate for nocturnal leg cramps concomitantly with chronic astemizole 10 mg/day. The concurrent use of QUALAQUIN with astemizole and other CYP3A4 substrates with QT prolongation potential (e.g., cisapride, terfenadine, halofantrine, pimozide and quinidine) should also be avoided [see Warnings and Precautions (5.3) ].. Atorvastatin (CYP3A4 substrate): Rhabdomyolysis with acute renal failure secondary to myoglobinuria was reported in patient taking atorvastatin administered with single dose of quinine. Quinine may increase plasma concentrations of atorvastatin, thereby increasing the risk of myopathy or rhabdomyolysis. Thus, clinicians considering combined therapy of QUALAQUIN with atorvastatin or other HMG-CoA reductase inhibitors (statins) that are CYP3A4 substrates (e.g., simvastatin, lovastatin) should carefully weigh the potential benefits and risks of each medication. If QUALAQUIN is used concomitantly with any of these statins, lower starting and maintenance doses of the statin should be considered. Patients should also be monitored closely for any signs or symptoms of muscle pain, tenderness, or weakness, particularly during initial therapy. If marked creatine phosphokinase (CPK) elevation occurs or myopathy (defined as muscle aches or muscle weakness in conjunction with CPK values >10 times the upper limit of normal) is diagnosed or suspected, atorvastatin or other statin should be discontinued.. Desipramine (CYP2D6 substrate): Quinine (750 mg/day for days) decreased the metabolism of desipramine in patients who were extensive CYP2D6 metabolizers, but had no effect in patients who were poor CYP2D6 metabolizers. Lower doses (80 mg to 400 mg) of quinine did not significantly affect the pharmacokinetics of other CYP2D6 substrates, namely, debrisoquine, dextromethorphan, and methoxyphenamine. Although clinical drug interaction studies have not been performed, antimalarial doses (greater than or equal to 600 mg) of quinine may inhibit the metabolism of other drugs that are CYP2D6 substrates (e.g., flecainide, debrisoquine, dextromethorphan, metoprolol, paroxetine). Patients taking medications that are CYP2D6 substrates with QUALAQUIN should be monitored closely for adverse reactions associated with these medications.. Digoxin (P-gp substrate): In healthy subjects who received digoxin (0.5 to 0.75 mg/day) during treatment with quinine (750 mg/day), 33% increase in mean steady state AUC of digoxin and 35% reduction in the steady state biliary clearance of digoxin were observed compared to digoxin alone. Thus, if QUALAQUIN is administered to patients receiving digoxin, plasma digoxin concentrations should be closely monitored, and the digoxin dose adjusted, as necessary [see Warnings and Precautions (5.7) ].. Halofantrine: Although not studied clinically, quinine was shown to inhibit the metabolism of halofantrine in vitro using human liver microsomes. Therefore, concomitant administration of QUALAQUIN is likely to increase plasma halofantrine concentrations [see Warnings and Precautions (5.3) ].. Mefloquine: In healthy subjects who received mefloquine (750 mg) at 24 hours before an oral 600 mg dose of quinine sulfate, the AUC of mefloquine was increased by 22% compared to mefloquine alone. In this study, the QTc interval was significantly prolonged in the subjects who received mefloquine and quinine sulfate 24 hours apart. The concomitant administration of mefloquine and QUALAQUIN may produce electrocardiographic abnormalities (including QTc prolongation) and may increase the risk of seizures [see Warnings and Precautions (5.3) ].. Midazolam (CYP3A4 substrate): In 23 healthy subjects who received multiple doses of QUALAQUIN 324 mg three times daily 7 days with single oral mg dose of midazolam, the mean AUC and Cmax of midazolam and 1-hydroxymidazolam were not significantly affected. This finding indicates that 7-day dosing with QUALAQUIN 324 mg every hours did not induce the metabolism of midazolam.. Neuromuscular blocking agents (pancuronium, succinylcholine, tubocurarine): In one report, quinine potentiated neuromuscular blockade in patient who received pancuronium during an operative procedure, and subsequently (3 hours after receiving pancuronium) received quinine 1800 mg daily. Quinine may also enhance the neuromuscular blocking effects of succinylcholine and tubocurarine [see Warnings and Precautions (5.5) ].. Ritonavir: In healthy subjects who received single oral 600 mg dose of quinine sulfate with the 15th dose of ritonavir (200 mg every 12 hours for days), the mean ritonavir AUC, Cmax, and elimination half-life were slightly but not significantly increased compared to when ritonavir was given alone. However, due to the significant effect of ritonavir on quinine pharmacokinetics, the concomitant administration of QUALAQUIN capsules with ritonavir should be avoided [see also Drug Interactions (7.1) ].. Theophylline or aminophylline (CYP1A2 substrate): In 19 healthy subjects who received multiple doses of QUALAQUIN 648 mg every hours 7 days with single 300 mg oral dose of theophylline, the mean theophylline AUC was 10% lower than when theophylline was given alone. There was no significant effect on mean theophylline Cmax. Therefore, if QUALAQUIN is co-administered to patients receiving theophylline or aminophylline, plasma theophylline concentrations should be monitored frequently to ensure therapeutic concentrations.. Warfarin and oral anticoagulants: Cinchona alkaloids, including quinine, may have the potential to depress hepatic enzyme synthesis of vitamin K-dependent coagulation pathway proteins and may enhance the action of warfarin and other oral anticoagulants. Quinine may also interfere with the anticoagulant effect of heparin. Thus, in patients receiving these anticoagulants, the prothrombin time (PT), partial thromboplastin time (PTT), or international normalization ratio (INR) should be closely monitored as appropriate, during concurrent therapy with QUALAQUIN.. 7.3 Drug/Laboratory Interactions. Quinine may produce an elevated value for urinary 17-ketogenic steroids when the Zimmerman method is used.Quinine may interfere with urine qualitative dipstick protein assays as well as quantitative methods (e.g., pyrogallol red-molybdate).

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics. AbsorptionThe oral bioavailability of quinine is 76 to 88% in healthy adults. Quinine exposure is higher in patients with malaria than in healthy subjects. After single oral dose of quinine sulfate, the mean quinine Tmax was longer, and mean AUC and Cmax were higher in patients with uncomplicated P. falciparum malaria than in healthy subjects, as shown in Table below.TABLE Pharmacokinetic Parameters of Quinine in Healthy Subjects and Patients with Uncomplicated P. falciparum Malaria after Single Dose of Oral Quinine Sulfate CapsulesHealthy Subjects(N 23)Mean +- SDUncomplicated P. falciparum Malaria Patients(N 15)Mean +- SDDose (mg/kg)Quinine Sulfate dose was 648 mg (approximately 8.7 mg/kg) in healthy subjects; and 10 mg/kg in patients with malaria 8.710Tmax (h)2.8 +- 0.85.9 +- 4.7Cmax (mcg/mL)3.2 +- 0.78.4AUC0-12 (mcgh/mL)28.073.0QUALAQUIN capsules may be administered without regard to meals. When single oral 324 mg capsule of QUALAQUIN was administered to healthy subjects (N=26) with standardized high-fat breakfast, the mean Tmax of quinine was prolonged to about 4.0 hours, but the mean Cmax and AUC0-24h were similar to those achieved when QUALAQUIN capsule was given under fasted conditions [see Dosage and Administration (2.1) ].. DistributionIn patients with malaria, the volume of distribution (Vd/F) decreases in proportion to the severity of the infection. In published studies with healthy subjects who received single oral 600 mg dose of quinine sulfate, the mean Vd/F ranged from 2.5 to 7.1 L/kg.Quinine is moderately protein-bound in blood in healthy subjects, ranging from 69 to 92%. During active malarial infection, protein binding of quinine is increased to 78 to 95%, corresponding to the increase in 1-acid glycoprotein that occurs with malaria infection.Intra-erythrocytic levels of quinine are approximately 30 to 50% of the plasma concentration.Quinine penetrates relatively poorly into the cerebrospinal fluid (CSF) in patients with cerebral malaria, with CSF concentration approximately to 7% of plasma concentration.In one study, quinine concentrations in placental cord blood and breast milk were approximately 32% and 31%, respectively, of quinine concentrations in maternal plasma. The estimated total dose of quinine secreted into breast milk was less than to mg per day [see Use in Specific Populations (8.1, 8.3) ].. MetabolismQuinine is metabolized almost exclusively via hepatic oxidative cytochrome P450 (CYP) pathways, resulting in four primary metabolites, 3-hydroxyquinine, 2-quinone, O-desmethylquinine, and 10,11-dihydroxydihydroquinine. Six secondary metabolites result from further biotransformation of the primary metabolites. The major metabolite, 3-hydroxyquinine, is less active than the parent drug.In vitro studies using human liver microsomes and recombinant P450 enzymes have shown that quinine is metabolized mainly by CYP3A4. Depending on the in vitro experimental conditions, other enzymes, including CYP1A2, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP2E1 were shown to have some role in the metabolism of quinine.. Elimination/ExcretionQuinine is eliminated primarily via hepatic biotransformation. Approximately 20% of quinine is excreted unchanged in urine. Because quinine is reabsorbed when the urine is alkaline, renal excretion of the drug is twice as rapid when the urine is acidic than when it is alkaline.In various published studies, healthy subjects who received single oral 600 mg dose of quinine sulfate exhibited mean plasma clearance ranging from 0.08 to 0.47 L/h/kg (median value: 0.17 L/h/kg) with mean plasma elimination half-life of 9.7 to 12.5 hours.In 15 patients with uncomplicated malaria who received 10 mg/kg oral dose of quinine sulfate, the mean total clearance of quinine was slower (approximately 0.09 L/h/kg) during the acute phase of the infection, and faster (approximately 0.16 L/h/kg) during the recovery or convalescent phase.. Extracorporeal Elimination: Administration of multiple-dose activated charcoal (50 grams administered hours after quinine dosing followed by further doses over the next 12 hours) decreased the mean quinine elimination half-life from 8.2 to 4.6 hours, and increased the mean quinine clearance by 56% (from 11.8 L/h to 18.4 L/h) in healthy adult subjects who received single oral 600 mg dose of quinine sulfate. Likewise, in symptomatic patients with acute quinine poisoning who received multiple-dose activated charcoal (50 grams every hours), the mean quinine elimination half-life was shortened to 8.1 hours in comparison to half-life of approximately 26 hours in patients who did not receive activated charcoal [see Overdosage (10) ].In patients with quinine poisoning, forced acid diuresis did not change the half-life of quinine elimination (25.1 +- 4.6 hours vs. 26.5 +- 5.8 hours), or the amount of unchanged quinine recovered in the urine, in comparison to patients not treated in this manner [see Overdosage (10) ].. Specific Populations. Pediatric Patients: The pharmacokinetics of quinine in children (1.5 to 12 years old) with uncomplicated P. falciparum malaria appear to be similar to that seen in adults with uncomplicated malaria. Furthermore, as seen in adults, the mean total clearance and the volume of distribution of quinine were reduced in pediatric patients with malaria as compared to the healthy pediatric controls. Table below provides comparison of the mean +- SD pharmacokinetic parameters of quinine in pediatric patients vs. healthy pediatric controls.TABLE Quinine Pharmacokinetic Parameters Following the First 10 mg/kg Quinine Sulfate Oral Dose in Healthy Pediatric Controls and Pediatric Patients with Acute Uncomplicated P. falciparum MalariaHealthy Pediatric Controlsage 1.5 to 12 years (N 5)Mean +- SDP. falciparum Malaria Pediatric Patients(N 15)Mean +- SDTmax (h)2.04.0Cmax (mcg/mL)3.4 +- 1.187.5 +- 1.1Half-life (h)3.2 +- 0.312.1 +- 1.4Total CL (L/h/kg)0.30 +- 0.040.06 +- 0.01Vd (L/kg)1.43 +- 0.180.87 +- 0.12. Geriatric Patients: Following single oral dose of 600 mg quinine sulfate, the mean AUC was about 38% higher in healthy elderly subjects (65 to 78 years old) than in 12 younger subjects (20 to 35 years old). The mean Tmax and Cmax were similar in elderly and younger subjects after single oral dose of quinine sulfate 600 mg. The mean oral clearance of quinine was significantly decreased, and the mean elimination half-life was significantly increased in elderly subjects compared with younger subjects (0.06 vs. 0.08 L/h/kg, and 18.4 hours vs. 10.5 hours, respectively). Although there was no significant difference in the renal clearance of quinine between the two age groups, elderly subjects excreted larger proportion of the dose in urine as unchanged drug than younger subjects (16.6% vs. 11.2%).After single 648 mg dose or at steady state, following quinine sulfate 648 mg given three times daily for days, no difference in the rate and extent of absorption or clearance of quinine was seen between 13 elderly subjects (65 to 78 years old) and 14 young subjects (20 to 39 years old). The mean elimination half-life was 20% longer in the elderly subjects (24.0 hours) than in younger subjects (20.0 hours). The steady state Cmax (+-SD) and AUC0-8 (+-SD) for healthy volunteers are 6.8 +- 1.24 mcg/mL and 48.8 +- 9.15 mcgh/mL, respectively, following days of oral quinine sulfate 648 mg three times daily. The steady state pharmacokinetic parameters in healthy elderly subjects were similar to the pharmacokinetic parameters in healthy young subjects.. Renal Impairment: Following single oral 600 mg dose of quinine sulfate in otherwise healthy subjects with severe chronic renal failure not receiving any form of dialysis (mean serum creatinine 9.6 mg/dL), the median AUC was higher by 195% and the median Cmax was higher by 79% than in subjects with normal renal function (mean serum creatinine 1 mg/dL). The mean plasma half-life in subjects with severe chronic renal impairment was prolonged to 26 hours compared to 9.7 hours in the healthy controls. Computer assisted modeling and simulation indicates that in patients with malaria and severe chronic renal failure, dosage regimen consisting of one loading dose of 648 mg QUALAQUIN followed 12 hours later by maintenance dosing regimen of 324 mg every 12 hours will provide adequate systemic exposure to quinine [see Dosage and Administration (2.2) ]. The effects of mild and moderate renal impairment on the pharmacokinetics and safety of quinine sulfate are not known.Negligible to minimal amounts of circulating quinine in the blood are removed by hemodialysis or hemofiltration. In subjects with chronic renal failure (CRF) on hemodialysis, only about 6.5% of quinine is removed in hour. Plasma quinine concentrations do not change during or shortly after hemofiltration in subjects with CRF [see Overdosage (10) ].. Hepatic Impairment: In otherwise healthy subjects with mild hepatic impairment (Child-Pugh A; N=10), who received single 500 mg dose of quinine sulfate, there was no significant difference in quinine pharmacokinetic parameters or exposure to the primary metabolite, 3-hydroxyquinine as compared to healthy controls (N=10). In otherwise healthy subjects with moderate hepatic impairment (Child-Pugh B; N=9) who received single oral 600 mg dose of quinine sulfate, the mean AUC increased by 55% without significant change in mean Cmax, as compared to healthy volunteer controls (N=6). In subjects with hepatitis, the absorption of quinine was prolonged, the elimination half-life was increased, the apparent volume of distribution was higher, but there was no significant difference in weight-adjusted clearance. Therefore, in patients with mild to moderate hepatic impairment, dosage adjustment is not needed, but patients should be monitored closely for adverse effects of quinine [see Use in Specific Populations (8.7) ].In subjects with severe hepatic impairment (Child-Pugh C; N=10), quinine oral clearance (CL/F) was reduced as was formation of the primary 3-hydroxyquinine metabolite. Volume of distribution (Vd/F) was higher and the plasma elimination half-life was increased. Therefore, quinine is not indicated in this population and alternate therapy should be administered [see Dosage and Administration (2.3) ].

PREGNANCY SECTION.

8.1 Pregnancy. Pregnancy Category CThere are extensive published data but few well-controlled studies of QUALAQUIN in pregnant women. Published data on over 1,000 pregnancy exposures to quinine did not show an increase in teratogenic effects over the background rate in the general population; however, the majority of these exposures were not in the first trimester. In developmental and reproductive toxicity studies, central nervous system (CNS) and ear abnormalities and increased fetal deaths occurred in some species when pregnant animals received quinine at doses about to times the human clinical dose. Quinine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.P. falciparum malaria carries higher risk of morbidity and mortality in pregnant women than in the general population. Pregnant women with P. falciparum malaria have an increased incidence of fetal loss (including spontaneous abortion and stillbirth), preterm labor and delivery, intrauterine growth retardation, low birth weight, and maternal death. Therefore, treatment of malaria in pregnancy is important.Hypoglycemia, due to increased pancreatic secretion of insulin, has been associated with quinine use, particularly in pregnant women.Quinine crosses the placenta with measurable blood concentrations in the fetus. In women who delivered live infants to days after starting quinine therapy, umbilical cord plasma quinine concentrations were between 1.0 and 4.6 mg/L (mean 2.4 mg/L) and the mean (+-SD) ratio of cord plasma to maternal plasma quinine concentrations was 0.32 +- 0.14. Quinine levels in the fetus may not be therapeutic. If congenital malaria is suspected after delivery, the infant should be evaluated and treated appropriately.A study from Thailand (1999) of women with P. falciparum malaria who were treated with oral quinine sulfate 10 mg/kg times daily for days at anytime in pregnancy reported no significant difference in the rate of stillbirths at >28 weeks of gestation in women treated with quinine (10 of 633 women [1.6%]) as compared with control group without malaria or exposure to antimalarial drugs during pregnancy (40 of 2201 women [1.8%]). The overall rate of congenital malformations (9 of 633 offspring [1.4%]) was not different for women who were treated with quinine sulfate compared with the control group (38 of 2201 offspring [1.7%]). The spontaneous abortion rate was higher in the control group (10.9%) than in women treated with quinine sulfate (3.5%) [OR 3.1; 95% CI 2.1-4.7]. An epidemiologic survey that included 104 mother-child pairs exposed to quinine during the first months of pregnancy, found no increased risk of structural birth defects was seen (2 fetal malformations [1.9%]). Rare and isolated case reports describe deafness and optic nerve hypoplasia in children exposed in utero due to maternal ingestion of high doses of quinine.In animal developmental studies conducted in multiple animal species, pregnant animals received quinine by the subcutaneous or intramuscular route at dose levels similar to the maximum recommended human dose (MRHD; 32 mg/kg/day) based on body surface area (BSA) comparisons. There were increases in fetal death in utero in rabbits at maternal doses >= 100 mg/kg/day and in dogs at >= 15 mg/kg/day corresponding to dose levels approximately 0.5 and 0.25 times the MRHD respectively based on BSA comparisons. Rabbit offspring had increased rates of degenerated auditory nerve and spiral ganglion and increased rates of CNS anomalies such as anencephaly and microcephaly at dose of 130 mg/kg/day corresponding to maternal dose approximately 1.3 times the MRHD based on BSA comparison. Guinea pig offspring had increased rates of hemorrhage and mitochondrial change in the cochlea at maternal doses of 200 mg/kg corresponding to dose level of approximately 1.4 times the MRHD based on BSA comparison. There were no teratogenic findings in rats at maternal doses up to 300 mg/kg/day and in monkeys at doses up to 200 mg/kg/day corresponding to doses approximately and times the MRHD respectively based on BSA comparisons.In pre- postnatal study in rats, an estimated oral dose of quinine sulfate of 20 mg/kg/day corresponding to approximately 0.1 times the MRHD based on BSA comparison resulted in offspring with impaired growth, lower body weights at birth and during the lactation period, and delayed physical development of teeth eruption and eye opening during the lactation period.

SPL MEDGUIDE SECTION.

MEDICATION GUIDEQUALAQUIN(R) (kwol-a-kwin)(Quinine sulfate) CapsulesRead the Medication Guide that comes with QUALAQUIN(R) before you start taking it and each time you get refill. There may be new information. This Medication Guide does not take the place of talking to your healthcare provider about your medical condition or treatment. You and your healthcare provider should talk about QUALAQUIN(R) when you start taking it and at regular checkups. QUALAQUIN(R) is not approved for the treatment of night-time leg cramps.What is the most important information should know about QUALAQUIN(R)QUALAQUIN(R) used to treat or prevent leg cramps may cause serious side effects or even death.QUALAQUIN(R) may cause your blood cell (platelet) count to drop causing serious bleeding problems. In some people, serious kidney problems can happen.QUALAQUIN(R) may cause problems with your heart rhythm that can lead to death.QUALAQUIN(R) may cause serious allergic reactions.Call your healthcare provider right away if you have:easy bruisingsevere nose bleedblood in urine or stoolbleeding gumsappearance of unusual purple, brown or red spots on your skin (bleeding under your skin)rashhivessevere itchingsevere flushingswelling of your facetrouble breathingchest painrapid heartbeatirregular heart rhythmweaknesssweatingnervousnessTaking QUALAQUIN(R) with some other medicines can increase the chance of serious side effects. Tell your healthcare provider if you take any other medicines.Certain medicines can cause the blood levels of QUALAQUIN(R) to be too high or too low in your body. It is important for you to tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins and herbal supplements. QUALAQUIN(R) and other medicines may affect each other causing serious side effects or death. Even medicines that you may take for short period of time, such as antibiotics, can mix in your blood with QUALAQUIN(R) and cause serious side effects or death. Do not start taking new medicine without telling your healthcare provider or pharmacist. What is QUALAQUIN(R)QUALAQUIN(R) is prescription medication used to treat malaria (uncomplicated) caused by the parasite Plasmodium falciparum. QUALAQUIN(R) is Not approved to:Prevent malariaTreat severe or complicated malariaPrevent or treat night-time leg crampsIt is not known if QUALAQUIN(R) is safe and works in children younger than 16 years old.Who should not take QUALAQUIN(R)Do not take QUALAQUIN(R) if you have:certain heart rhythm problems (atrial fibrillation) or abnormal electrocardiogram (ECG) (QT prolongation).low levels of an enzyme called Glucose-6-phosphate dehydrogenase (G6PD).an autoimmune disease (myasthenia gravis) that leads to muscle weakness.had allergic reactions to quinine, quinidine, or mefloquine (Lariam(R)).had serious side effects to quinine (QUALAQUIN(R)), such as low platelets, which are necessary for your blood to clot.an inflammation of the nerve important for vision (optic neuritis).What should tell my healthcare provider before starting QUALAQUIN(R)Before you take QUALAQUIN(R), tell your healthcare provider if you:Have heart problems.Have kidney problems.Have liver problems.Have any other medical condition.Are pregnant or could be pregnant. Treatment of malaria is important because it can be serious disease for pregnant woman and her unborn baby. Your healthcare provider can tell you more about the benefits and risks of taking this medication during pregnancy. Low blood sugar (hypoglycemia) can be seen in pregnant women while taking QUALAQUIN(R). This can include sweating, weakness, nausea, vomiting, or confusion. You and your healthcare provider can decide if QUALAQUIN(R) is right for you.Are breast-feeding. Small amounts of QUALAQUIN(R) can pass into your breast milk. You and your healthcare provider can decide if you should breastfeed while taking QUALAQUIN(R).Tell your healthcare provider about all the medicines you take, including prescription medicines, vitamins and herbal supplements.How should take QUALAQUIN(R)Take QUALAQUIN(R) exactly as your healthcare provider tells you to take it.Your healthcare provider will tell you how many QUALAQUIN(R) capsules to take and when to take them.To lower the chance of stomach upset, take QUALAQUIN(R) with food.Finish all the QUALAQUIN(R) that is prescribed even if you feel better. Do not stop taking the medication without talking to your healthcare provider.Do not take more than the amount prescribed. Do not take more than capsules at one time or more than doses in one day. If you take more than the prescribed dose, call your healthcare provider right away.If you forget to take QUALAQUIN(R), do not double the next dose. If it has been more than hours since the missed dose, just wait and take the regular dose at the next scheduled time. Call your healthcare provider if you are not sure what to do.If you take too much QUALAQUIN(R), call your healthcare provider or go to the nearest emergency room right away.Call your healthcare provider right away if:If you feel worse, or if you do not start feeling better within or days of starting to take QUALAQUIN(R).If your fever comes back after finishing treatment with QUALAQUIN(R).What are the possible side effects of QUALAQUIN(R)QUALAQUIN(R) may cause serious side effects.See What is the most important information should know about QUALAQUIN (R) section.Low blood sugar (hypoglycemia). This can include sweating, weakness, nausea, vomiting, or confusion.Common side effects with QUALAQUIN(R) include:headachesweatingflushingnausearinging in your earsdiarrheadeafnesshearing lossdizziness (vertigo)blurred visionchanges in how you see colorvomitingstomach painblindnessTell your healthcare provider if you have any side effect that bothers you or that does not go away.These are not all of the possible side effects of QUALAQUIN(R). For more information, ask your healthcare provider or pharmacist.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should store QUALAQUIN(R)Keep the capsules in tightly closed container.Do not refrigerate or freeze.Store at 20C to 25C (68oF to 77F).Keep QUALAQUIN(R) and all medicines out of the reach of children.General Information about QUALAQUIN(R) Medicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use QUALAQUIN(R) for condition for which it was not prescribed. Do not give QUALAQUIN(R) to other people, even if they have the same symptoms that you have. It may harm them.This Medication Guide summarizes the most important information about QUALAQUIN(R). If you would like more information, talk with your healthcare provider. You can ask your healthcare provider or pharmacist for information about QUALAQUIN(R) that is written for healthcare professionals.For more information, go to www.QUALAQUIN.com or call 1-888-351-3786.What are the ingredients in QUALAQUIN(R)Active Ingredients: Quinine Sulfate, USP Inactive Ingredients: Corn starch, magnesium stearate, talcThis Medication Guide has been approved by the U.S. Food and Drug Administration.Manufactured for:AR SCIENTIFIC, INC.Philadelphia, PA 19124 USAby:MUTUAL PHARMACEUTICAL COMPANY, INC.Philadelphia, PA 19124 USARev 23, April 2013. QUALAQUIN(R) may cause your blood cell (platelet) count to drop causing serious bleeding problems. In some people, serious kidney problems can happen.. QUALAQUIN(R) may cause problems with your heart rhythm that can lead to death.. QUALAQUIN(R) may cause serious allergic reactions.. easy bruising. severe nose bleed. blood in urine or stool. bleeding gums. appearance of unusual purple, brown or red spots on your skin (bleeding under your skin). rash. hives. severe itching. severe flushing. swelling of your face. trouble breathing. chest pain. rapid heartbeat. irregular heart rhythm. weakness. sweating. nervousness. Prevent malaria. Treat severe or complicated malaria. Prevent or treat night-time leg cramps. certain heart rhythm problems (atrial fibrillation) or abnormal electrocardiogram (ECG) (QT prolongation).. low levels of an enzyme called Glucose-6-phosphate dehydrogenase (G6PD).. an autoimmune disease (myasthenia gravis) that leads to muscle weakness.. had allergic reactions to quinine, quinidine, or mefloquine (Lariam(R)).. had serious side effects to quinine (QUALAQUIN(R)), such as low platelets, which are necessary for your blood to clot.. an inflammation of the nerve important for vision (optic neuritis).. Have heart problems.. Have kidney problems.. Have liver problems.. Have any other medical condition.. Are pregnant or could be pregnant. Treatment of malaria is important because it can be serious disease for pregnant woman and her unborn baby. Your healthcare provider can tell you more about the benefits and risks of taking this medication during pregnancy. Low blood sugar (hypoglycemia) can be seen in pregnant women while taking QUALAQUIN(R). This can include sweating, weakness, nausea, vomiting, or confusion. You and your healthcare provider can decide if QUALAQUIN(R) is right for you.. Are breast-feeding. Small amounts of QUALAQUIN(R) can pass into your breast milk. You and your healthcare provider can decide if you should breastfeed while taking QUALAQUIN(R).. Take QUALAQUIN(R) exactly as your healthcare provider tells you to take it.. Your healthcare provider will tell you how many QUALAQUIN(R) capsules to take and when to take them.. To lower the chance of stomach upset, take QUALAQUIN(R) with food.. Finish all the QUALAQUIN(R) that is prescribed even if you feel better. Do not stop taking the medication without talking to your healthcare provider.. Do not take more than the amount prescribed. Do not take more than capsules at one time or more than doses in one day. If you take more than the prescribed dose, call your healthcare provider right away.. If you forget to take QUALAQUIN(R), do not double the next dose. If it has been more than hours since the missed dose, just wait and take the regular dose at the next scheduled time. Call your healthcare provider if you are not sure what to do.. If you take too much QUALAQUIN(R), call your healthcare provider or go to the nearest emergency room right away.. If you feel worse, or if you do not start feeling better within or days of starting to take QUALAQUIN(R).. If your fever comes back after finishing treatment with QUALAQUIN(R).. See What is the most important information should know about QUALAQUIN (R) section.. Low blood sugar (hypoglycemia). This can include sweating, weakness, nausea, vomiting, or confusion.. headache. sweating. flushing. nausea. ringing in your ears. diarrhea. deafness. hearing loss. dizziness (vertigo). blurred vision. changes in how you see color. vomiting. stomach pain. blindness. Keep the capsules in tightly closed container.. Do not refrigerate or freeze.. Store at 20C to 25C (68oF to 77F).

TERATOGENIC EFFECTS SECTION.

Pregnancy Category CThere are extensive published data but few well-controlled studies of QUALAQUIN in pregnant women. Published data on over 1,000 pregnancy exposures to quinine did not show an increase in teratogenic effects over the background rate in the general population; however, the majority of these exposures were not in the first trimester. In developmental and reproductive toxicity studies, central nervous system (CNS) and ear abnormalities and increased fetal deaths occurred in some species when pregnant animals received quinine at doses about to times the human clinical dose. Quinine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.P. falciparum malaria carries higher risk of morbidity and mortality in pregnant women than in the general population. Pregnant women with P. falciparum malaria have an increased incidence of fetal loss (including spontaneous abortion and stillbirth), preterm labor and delivery, intrauterine growth retardation, low birth weight, and maternal death. Therefore, treatment of malaria in pregnancy is important.Hypoglycemia, due to increased pancreatic secretion of insulin, has been associated with quinine use, particularly in pregnant women.Quinine crosses the placenta with measurable blood concentrations in the fetus. In women who delivered live infants to days after starting quinine therapy, umbilical cord plasma quinine concentrations were between 1.0 and 4.6 mg/L (mean 2.4 mg/L) and the mean (+-SD) ratio of cord plasma to maternal plasma quinine concentrations was 0.32 +- 0.14. Quinine levels in the fetus may not be therapeutic. If congenital malaria is suspected after delivery, the infant should be evaluated and treated appropriately.A study from Thailand (1999) of women with P. falciparum malaria who were treated with oral quinine sulfate 10 mg/kg times daily for days at anytime in pregnancy reported no significant difference in the rate of stillbirths at >28 weeks of gestation in women treated with quinine (10 of 633 women [1.6%]) as compared with control group without malaria or exposure to antimalarial drugs during pregnancy (40 of 2201 women [1.8%]). The overall rate of congenital malformations (9 of 633 offspring [1.4%]) was not different for women who were treated with quinine sulfate compared with the control group (38 of 2201 offspring [1.7%]). The spontaneous abortion rate was higher in the control group (10.9%) than in women treated with quinine sulfate (3.5%) [OR 3.1; 95% CI 2.1-4.7]. An epidemiologic survey that included 104 mother-child pairs exposed to quinine during the first months of pregnancy, found no increased risk of structural birth defects was seen (2 fetal malformations [1.9%]). Rare and isolated case reports describe deafness and optic nerve hypoplasia in children exposed in utero due to maternal ingestion of high doses of quinine.In animal developmental studies conducted in multiple animal species, pregnant animals received quinine by the subcutaneous or intramuscular route at dose levels similar to the maximum recommended human dose (MRHD; 32 mg/kg/day) based on body surface area (BSA) comparisons. There were increases in fetal death in utero in rabbits at maternal doses >= 100 mg/kg/day and in dogs at >= 15 mg/kg/day corresponding to dose levels approximately 0.5 and 0.25 times the MRHD respectively based on BSA comparisons. Rabbit offspring had increased rates of degenerated auditory nerve and spiral ganglion and increased rates of CNS anomalies such as anencephaly and microcephaly at dose of 130 mg/kg/day corresponding to maternal dose approximately 1.3 times the MRHD based on BSA comparison. Guinea pig offspring had increased rates of hemorrhage and mitochondrial change in the cochlea at maternal doses of 200 mg/kg corresponding to dose level of approximately 1.4 times the MRHD based on BSA comparison. There were no teratogenic findings in rats at maternal doses up to 300 mg/kg/day and in monkeys at doses up to 200 mg/kg/day corresponding to doses approximately and times the MRHD respectively based on BSA comparisons.In pre- postnatal study in rats, an estimated oral dose of quinine sulfate of 20 mg/kg/day corresponding to approximately 0.1 times the MRHD based on BSA comparison resulted in offspring with impaired growth, lower body weights at birth and during the lactation period, and delayed physical development of teeth eruption and eye opening during the lactation period.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Renal impairment: Reduce dose and dosing frequency for patients with severe chronic renal impairment (2.2, 8.6, 12.3).Hepatic impairment: Closely monitor for adverse events. Quinine should not be administered in patients with severe (Child-Pugh C) hepatic impairment (2.3, 8.7, 12.3).Pregnancy: Based on animal data may cause fetal harm. Use only if the potential benefit justifies the risk (8.1).Nursing Mothers: Exercise caution when administering to nursing woman (8.3).. Renal impairment: Reduce dose and dosing frequency for patients with severe chronic renal impairment (2.2, 8.6, 12.3).. Hepatic impairment: Closely monitor for adverse events. Quinine should not be administered in patients with severe (Child-Pugh C) hepatic impairment (2.3, 8.7, 12.3).. Pregnancy: Based on animal data may cause fetal harm. Use only if the potential benefit justifies the risk (8.1).. Nursing Mothers: Exercise caution when administering to nursing woman (8.3).. 8.1 Pregnancy. Pregnancy Category CThere are extensive published data but few well-controlled studies of QUALAQUIN in pregnant women. Published data on over 1,000 pregnancy exposures to quinine did not show an increase in teratogenic effects over the background rate in the general population; however, the majority of these exposures were not in the first trimester. In developmental and reproductive toxicity studies, central nervous system (CNS) and ear abnormalities and increased fetal deaths occurred in some species when pregnant animals received quinine at doses about to times the human clinical dose. Quinine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.P. falciparum malaria carries higher risk of morbidity and mortality in pregnant women than in the general population. Pregnant women with P. falciparum malaria have an increased incidence of fetal loss (including spontaneous abortion and stillbirth), preterm labor and delivery, intrauterine growth retardation, low birth weight, and maternal death. Therefore, treatment of malaria in pregnancy is important.Hypoglycemia, due to increased pancreatic secretion of insulin, has been associated with quinine use, particularly in pregnant women.Quinine crosses the placenta with measurable blood concentrations in the fetus. In women who delivered live infants to days after starting quinine therapy, umbilical cord plasma quinine concentrations were between 1.0 and 4.6 mg/L (mean 2.4 mg/L) and the mean (+-SD) ratio of cord plasma to maternal plasma quinine concentrations was 0.32 +- 0.14. Quinine levels in the fetus may not be therapeutic. If congenital malaria is suspected after delivery, the infant should be evaluated and treated appropriately.A study from Thailand (1999) of women with P. falciparum malaria who were treated with oral quinine sulfate 10 mg/kg times daily for days at anytime in pregnancy reported no significant difference in the rate of stillbirths at >28 weeks of gestation in women treated with quinine (10 of 633 women [1.6%]) as compared with control group without malaria or exposure to antimalarial drugs during pregnancy (40 of 2201 women [1.8%]). The overall rate of congenital malformations (9 of 633 offspring [1.4%]) was not different for women who were treated with quinine sulfate compared with the control group (38 of 2201 offspring [1.7%]). The spontaneous abortion rate was higher in the control group (10.9%) than in women treated with quinine sulfate (3.5%) [OR 3.1; 95% CI 2.1-4.7]. An epidemiologic survey that included 104 mother-child pairs exposed to quinine during the first months of pregnancy, found no increased risk of structural birth defects was seen (2 fetal malformations [1.9%]). Rare and isolated case reports describe deafness and optic nerve hypoplasia in children exposed in utero due to maternal ingestion of high doses of quinine.In animal developmental studies conducted in multiple animal species, pregnant animals received quinine by the subcutaneous or intramuscular route at dose levels similar to the maximum recommended human dose (MRHD; 32 mg/kg/day) based on body surface area (BSA) comparisons. There were increases in fetal death in utero in rabbits at maternal doses >= 100 mg/kg/day and in dogs at >= 15 mg/kg/day corresponding to dose levels approximately 0.5 and 0.25 times the MRHD respectively based on BSA comparisons. Rabbit offspring had increased rates of degenerated auditory nerve and spiral ganglion and increased rates of CNS anomalies such as anencephaly and microcephaly at dose of 130 mg/kg/day corresponding to maternal dose approximately 1.3 times the MRHD based on BSA comparison. Guinea pig offspring had increased rates of hemorrhage and mitochondrial change in the cochlea at maternal doses of 200 mg/kg corresponding to dose level of approximately 1.4 times the MRHD based on BSA comparison. There were no teratogenic findings in rats at maternal doses up to 300 mg/kg/day and in monkeys at doses up to 200 mg/kg/day corresponding to doses approximately and times the MRHD respectively based on BSA comparisons.In pre- postnatal study in rats, an estimated oral dose of quinine sulfate of 20 mg/kg/day corresponding to approximately 0.1 times the MRHD based on BSA comparison resulted in offspring with impaired growth, lower body weights at birth and during the lactation period, and delayed physical development of teeth eruption and eye opening during the lactation period.. 8.2 Labor and Delivery. There is no evidence that quinine causes uterine contractions at the doses recommended for the treatment of malaria. In doses several-times higher than those used to treat malaria, quinine may stimulate the pregnant uterus.. 8.3 Nursing Mothers. There is limited information on the safety of quinine in breastfed infants. No toxicity was reported in infants in single study where oral quinine sulfate (10 mg/kg every hours for to 10 days) was administered to 25 lactating women. It is estimated from this study that breastfed infants would receive less than to mg per day of quinine base (< 0.4% of the maternal dose) via breast milk [see Clinical Pharmacology (12.3) ].Although quinine is generally considered compatible with breastfeeding, the risks and benefits to infant and mother should be assessed. Caution should be exercised when administered to nursing woman.If malaria is suspected in the infant, appropriate evaluation and treatment should be provided. Plasma quinine levels may not be therapeutic in infants of nursing mothers receiving QUALAQUIN.. 8.4 Pediatric Use. The safety and efficacy of QUALAQUIN in pediatric patients under the age of 16 has not been established.. 8.5 Geriatric Use. Clinical studies of quinine sulfate did not include sufficient numbers of subjects aged 65 and over to determine whether they respond to treatment differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.. 8.6 Renal Impairment. Clearance of quinine is decreased in patients with severe chronic renal failure. The dosage and dosing frequency should be reduced [see Dosage and Administration (2.2), Clinical Pharmacology (12.3) ].. 8.7 Hepatic Impairment. In patients with severe hepatic impairment (Child-Pugh C), quinine oral clearance (CL/F) is decreased, volume of distribution (Vd/F) is increased, and half-life is prolonged, relative to subjects with normal liver function. Therefore, quinine is not indicated in patients with severe hepatic impairment and alternate therapy should be administered [see Dosage and Administration (2.3) and Clinical Pharmacology (12.3) ].Close monitoring is recommended for patients with mild (Child-Pugh A) or moderate (Child-Pugh B) hepatic impairment, as exposure to quinine may be increased relative to subjects with normal liver function [see Clinical Pharmacology (12.3) ].

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. Not indicated for the prevention or treatment of nocturnal leg cramps. Risk of serious and life-threatening adverse reactions (1, 5.1).Thrombocytopenia, including ITP and HUS/TTP, has been reported. Discontinue drug (5.2).QT prolongation and ventricular arrhythmias. Avoid concomitant use with drugs known to prolong QT interval (5.3).Avoid concomitant use with rifampin. QUALAQUIN treatment failures have been reported (5.4).Avoid concomitant use with neuromuscular blocking agents. QUALAQUIN may potentiate neuromuscular blockade and cause respiratory depression (5.5).Serious and life threatening hypersensitivity reactions. Discontinue drug (4, 5.6).Atrial fibrillation and flutter. Paradoxical increase in ventricular rate may occur. Closely monitor digoxin levels if used concomitantly (5.7).Hypoglycemia. Monitor for signs and symptoms (5.8).. Not indicated for the prevention or treatment of nocturnal leg cramps. Risk of serious and life-threatening adverse reactions (1, 5.1).. Thrombocytopenia, including ITP and HUS/TTP, has been reported. Discontinue drug (5.2).. QT prolongation and ventricular arrhythmias. Avoid concomitant use with drugs known to prolong QT interval (5.3).. Avoid concomitant use with rifampin. QUALAQUIN treatment failures have been reported (5.4).. Avoid concomitant use with neuromuscular blocking agents. QUALAQUIN may potentiate neuromuscular blockade and cause respiratory depression (5.5).. Serious and life threatening hypersensitivity reactions. Discontinue drug (4, 5.6).. Atrial fibrillation and flutter. Paradoxical increase in ventricular rate may occur. Closely monitor digoxin levels if used concomitantly (5.7).. Hypoglycemia. Monitor for signs and symptoms (5.8).. 5.1 Use of QUALAQUIN for Treatment or Prevention of Nocturnal Leg Cramps. QUALAQUIN may cause unpredictable serious and life-threatening hematologic reactions including thrombocytopenia and hemolytic-uremic syndrome/thrombotic thrombocytopenic purpura (HUS/TTP) in addition to hypersensitivity reactions, QT prolongation, serious cardiac arrhythmias including torsades de pointes, and other serious adverse events requiring medical intervention and hospitalization. Chronic renal impairment associated with the development of TTP, and fatalities have also been reported. The risk associated with the use of QUALAQUIN in the absence of evidence of its effectiveness for treatment or prevention of nocturnal leg cramps, outweighs any potential benefit in treating and/or preventing this benign, self-limiting condition [see Boxed Warning and Contraindications (4)].. 5.2 Thrombocytopenia. Quinine-induced thrombocytopenia is an immune-mediated disorder. Severe cases of thrombocytopenia that are fatal or life threatening have been reported, including cases of HUS/TTP. Chronic renal impairment associated with the development of TTP has also been reported. Thrombocytopenia usually resolves within week upon discontinuation of quinine. If quinine is not stopped, patient is at risk for fatal hemorrhage. Upon re-exposure to quinine from any source, patient with quinine-dependent antibodies could develop thrombocytopenia that is more rapid in onset and more severe than the original episode.. 5.3 QT Prolongation and Ventricular Arrhythmias QT interval prolongation has been consistent finding in studies which evaluated electrocardiographic changes with oral or parenteral quinine administration, regardless of age, clinical status, or severity of disease. The maximum increase in QT interval has been shown to correspond with peak quinine plasma concentration [see Clinical Pharmacology (12.2) ]. Quinine sulfate has been rarely associated with potentially fatal cardiac arrhythmias, including torsades de pointes, and ventricular fibrillation.QUALAQUIN has been shown to cause concentration-dependent prolongation of the PR and QRS interval. At particular risk are patients with underlying structural heart disease and preexisting conduction system abnormalities, elderly patients with sick sinus syndrome, patients with atrial fibrillation with slow ventricular response, patients with myocardial ischemia or patients receiving drugs known to prolong the PR interval (e.g. verapamil) or QRS interval (e.g. flecainide or quinidine) [see Clinical Pharmacology (12.2) ].QUALAQUIN is not recommended for use with other drugs known to cause QT prolongation, including Class IA antiarrhythmic agents (e.g., quinidine, procainamide, disopyramide), and Class III antiarrhythmic agents (e.g., amiodarone, sotalol, dofetilide).The use of macrolide antibiotics such as erythromycin should be avoided in patients receiving QUALAQUIN. Fatal torsades de pointes was reported in an elderly patient who received concomitant quinine, erythromycin, and dopamine. Although causal relationship between specific drug and the arrhythmia was not established in this case, erythromycin is CYP3A4 inhibitor and has been shown to increase quinine plasma levels when used concomitantly. related macrolide antibiotic, troleandomycin, has also been shown to increase quinine exposure in pharmacokinetic study [see Drug Interactions (7.1) ].Quinine may inhibit the metabolism of certain drugs that are CYP3A4 substrates and are known to cause QT prolongation, e.g., astemizole, cisapride, terfenadine, pimozide, halofantrine and quinidine. Torsades de pointes has been reported in patients who received concomitant quinine and astemizole. Therefore, concurrent use of QUALAQUIN with these medications, or drugs with similar properties, should be avoided [see Drug Interactions (7.2) ].Concomitant administration of QUALAQUIN with the antimalarial drugs, mefloquine or halofantrine, may result in electrocardiographic abnormalities, including QT prolongation, and increase the risk for torsades de pointes or other serious ventricular arrhythmias. Concurrent use of QUALAQUIN and mefloquine may also increase the risk of seizures [see Drug Interactions (7.2) ].QUALAQUIN should also be avoided in patients with known prolongation of QT interval and in patients with clinical conditions known to prolong the QT interval, such as uncorrected hypokalemia, bradycardia, and certain cardiac conditions [see Contraindications (4) ].. 5.4 Concomitant Use of Rifampin. Treatment failures may result from the concurrent use of rifampin with QUALAQUIN, due to decreased plasma concentrations of quinine, and concomitant use of these medications should be avoided [see Drug Interactions (7.1) ].. 5.5 Concomitant Use of Neuromuscular Blocking Agents. The use of neuromuscular blocking agents should be avoided in patients receiving QUALAQUIN. In one patient who received pancuronium during an operative procedure, subsequent administration of quinine resulted in respiratory depression and apnea. Although there are no clinical reports with succinylcholine or tubocurarine, quinine may also potentiate neuromuscular blockade when used with these drugs [see Drug Interactions (7.2) ].. 5.6 Hypersensitivity. Serious hypersensitivity reactions reported with quinine sulfate include anaphylactic shock, anaphylactoid reactions, urticaria, serious skin rashes, including Stevens-Johnson syndrome and toxic epidermal necrolysis, angioedema, facial edema, bronchospasm, and pruritus.A number of other serious adverse reactions reported with quinine, including thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS), thrombocytopenia, immune thrombocytopenic purpura (ITP), blackwater fever, disseminated intravascular coagulation, leukopenia, neutropenia, granulomatous hepatitis, and acute interstitial nephritis may also be due to hypersensitivity reactions.QUALAQUIN should be discontinued in case of any signs or symptoms of hypersensitivity [see Contraindications (4) ].. 5.7 Atrial Fibrillation and Flutter. QUALAQUIN should be used with caution in patients with atrial fibrillation or atrial flutter. paradoxical increase in ventricular response rate may occur with quinine, similar to that observed with quinidine. If digoxin is used to prevent rapid ventricular response, serum digoxin levels should be closely monitored, because digoxin levels may be increased with use of quinine [see Drug Interactions (7.2) ].. 5.8 Hypoglycemia. Quinine stimulates release of insulin from the pancreas, and patients, especially pregnant women, may experience clinically significant hypoglycemia.