ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS THE MAJOR TOXICITY OF FOSCARNET SODIUM INJECTION IS RENAL IMPAIRMENT (see WARNINGS section). Approximately 33% of 189 patients with AIDS and CMV retinitis who received foscarnet sodium Injection (60 mg/kg TID), without adequate hydration, developed significant impairment of renal function (serum creatinine >= 2.0 mg/dL). The incidence of renal impairment in subsequent clinical trials in which 1000 mL of normal saline or 5% dextrose solution was given with each infusion of foscarnet sodium Injection was 12% (34/280).Foscarnet sodium injection has been associated with changes in serum electrolytes including hypocalcemia (15 30%), hypophosphatemia (8 26%) and hyperphosphatemia (6%), hypomagnesemia (15 30%), and hypokalemia (16 48%) (see WARNINGS section). The higher percentages were derived from those patients receiving hydration.Foscarnet sodium injection treatment was associated with seizures in 18/189 (10%) AIDS patients in the initial five controlled studies (see WARNINGS section). Risk factors associated with seizures included impaired baseline renal function, low total serum calcium, and underlying CNS conditions predisposing the patient to seizures. The rate of seizures did not increase with duration of treatment. Three cases were associated with overdoses of foscarnet sodium Injection (see OVERDOSAGE section).In five controlled U.S. clinical trials the most frequently reported adverse events in patients with AIDS and CMV retinitis are shown in TABLE 9. These figures were calculated without reference to drug relationship or severity.TABLE Adverse Events Reported in Five Controlled US Clinical Trialsn 189n 189Fever65%Abnormal Renal Function27%Nausea47%Vomiting26%Anemia33%Headache26%Diarrhea30%Seizures10%From the same controlled studies, adverse events categorized by investigator as severe are shown in TABLE 10. Although death was specifically attributed to foscarnet sodium Injection in only one case, other complications of foscarnet sodium Injection (i.e., renal impairment, electrolyte abnormalities, and seizures) may have contributed to patient deaths (see WARNINGS section).TABLE 10 Severe Adverse Eventsn 189Death14%Abnormal Renal Function14%Marrow Suppression10%Anemia9%Seizures7%From the five initial U.S. controlled trials of foscarnet sodium Injection, the following list of adverse events has been compiled regardless of causal relationship to foscarnet sodium Injection. Evaluation of these reports was difficult because of the diverse manifestations of the underlying disease and because most patients received numerous concomitant medications.. Incidence of 5% or Greater Body as Whole: fever, fatigue, rigors, asthenia, malaise, pain, infection, sepsis, death Central and Peripheral Nervous System: headache, paresthesia, dizziness, involuntary muscle contractions, hypoesthesia, neuropathy, seizures including grand mal seizures (see WARNINGS)Gastrointestinal System: anorexia, nausea, diarrhea, vomiting, abdominal pain Hematologic: anemia, granulocytopenia, leukopenia, neutropenia (see PRECAUTIONS) Metabolic and Nutritional: mineral and electrolyte imbalances (see WARNINGS) including hypokalemia, hypocalcemia, hypomagnesemia, hypophosphatemia, hyperphosphatemia Psychiatric: depression, confusion, anxietyRespiratory System: coughing, dyspneaSkin and Appendages: rash, increased sweatingUrinary System: alterations in renal function including increased serum creatinine, decreased creatinine clearance, and abnormal renal function (see WARNINGS)Special Senses: vision abnormalities. Incidence between 1% and 5% Application Site: injection site pain, injection site inflammationBody as Whole: back pain, chest pain (including reports of transient chest pain as part of infusion reactions), edema, influenza-like symptoms, bacterial infections, moniliasis, fungal infections, abscessCardiovascular: hypertension, palpitations, ECG abnormalities including sinus tachycardia, first degree AV block and non-specific ST-T segment changes, hypotension, flushing, cerebrovascular disorder (see WARNINGS)Central and Peripheral Nervous System: tremor, ataxia, dementia, stupor, generalized spasms, sensory disturbances, meningitis, aphasia, abnormal coordination, leg cramps, EEG abnormalities (see WARNINGS)Gastrointestinal: constipation, dysphagia, dyspepsia, rectal hemorrhage, dry mouth, melena, flatulence, ulcerative stomatitis, pancreatitisHematologic: thrombocytopenia, platelet abnormalities, thrombosis, white blood cell abnormalities, lymphadenopathyLiver and Biliary: abnormal A-G ratio, abnormal hepatic function, increased SGPT, increased SGOTMetabolic and Nutritional: hyponatremia, decreased weight, increased alkaline phosphatase, increased LDH, increased BUN, acidosis, cachexia, thirst Musculo-Skeletal: arthralgia, myalgiaNeoplasms: lymphoma-like disorder, sarcomaPsychiatric: insomnia, somnolence, nervousness, amnesia, agitation, aggressive reaction, hallucinationRespiratory System: pneumonia, sinusitis, pharyngitis, rhinitis, respiratory disorders, respiratory insufficiency, pulmonary infiltration, stridor, pneumothorax, hemoptysis, bronchospasmSkin and Appendages: pruritus, skin ulceration, seborrhea, erythematous rash, maculopapular rash, skin discolorationSpecial Senses: taste perversions, eye abnormalities, eye pain, conjunctivitisUrinary System: albuminuria, dysuria, polyuria, urethral disorder, urinary retention, urinary tract infections, acute renal failure, nocturia, facial edema Selected adverse events occurring at rate of less than 1% in the five initial U.S. controlled clinical trials of foscarnet sodium Injection include: syndrome of inappropriate antidiuretic hormone secretion, pancytopenia, hematuria, dehydration, hypoproteinemia, increases in amylase and creatinine phosphokinase, cardiac arrest, coma, and other cardiovascular and neurologic complications.Selected adverse event data from the Foscarnet vs. Ganciclovir CMV Retinitis Trial (FGCRT), performed by the Studies of the Ocular Complications of AIDS (SOCA) Research Group, are shown in TABLE 11 (see CLINICAL TRIALS section).TABLE 11 FGCRT: Selected Adverse EventsValues for the treatment groups refer only to patients who completed at least one follow-up visit i.e., 133 to 119 patients in the ganciclovir group and 93 to 100 in the foscarnet group. Events denotes all events observed and patients the number of patients with one or more of the indicated events. EVENTGANCICLOVIRFOSCARNETNo. of EventsNo. ofPatientsRatesPer person-year at risk No. of EventsNo. ofPatientsRates Absolute neutrophil countdecreasing to <0.50 109 per liter63411.3031170.72Serum creatinine increasing to >260 umol per liter (>2.9 mg/dL)640.121390.30Seizure Final frozen SOCA database dated October 1991 21130.3719130.37Catheterization-related infection49271.2651281.46Hospitalization209914.74202755.03Selected adverse events from ACTG Study 228 (CRRT) comparing combination therapy with foscarnet sodium Injection or ganciclovir monotherapy are shown in TABLE 12. The most common reason for treatment change in patients assigned to either foscarnet sodium Injection or ganciclovir was retinitis progression. The most frequent reason for treatment change in the combination treatment group was toxicity.TABLE 12 CRRT: Selected Adverse EventsFoscarnet Sodium InjectionN=88GanciclovirN=93CombinationN=93No.No.RateRate events/person/year; No.No.Rate No.No.Rate EventsPts.Pts. patients with event; EventsPts. EventsPts. Anemia (Hgb <70g/L)1170.20970.1419150.33NeutropeniaANC absolute neutrophil count. ANC <0.75 109 cells/L86321.5395411.51107511.91ANC <0.50 109 cells/L50250.9149280.8050280.85ThrombocytopeniaPlatelets <50 109/L28140.501980.4340150.56Platelets <20 109/L110.01620.05760.18Nephrotoxicity1070.1711100.20Creatinine >260 umol/L (>2.9 mg/dL)970.15Seizures660.17760.151050.18Hospitalizations86531.86111592.36118642.36Adverse events that have been reported in post-marketing surveillance include: administration site extravasation, localized edema, hypersensitivity reactions (including anaphylactic shock, urticaria and angioedema) (see WARNINGS section), gastrointestinal hemorrhage, increased lipase, glomerulonephritis, nephrotic syndrome, proteinuria, status epilepticus, ventricular arrhythmia, prolongation of QT interval, torsade de pointes (see WARNINGS section), gamma GT increased, diabetes insipidus (usually nephrogenic), renal calculus, Fanconi syndrome acquired, renal tubular acidosis, renal tubular necrosis, crystal-induced nephropathy, hypercalcemia, hypernatremia, esophageal ulceration and muscle disorders including myopathy, myositis, muscle weakness and rare cases of rhabdomyolysis. Cases of vesiculobullous eruptions including erythema multiforme, toxic epidermal necrolysis, and Stevens-Johnson syndrome have been reported. In most cases, patients were taking other medications that have been associated with toxic epidermal necrolysis or Stevens-Johnson syndrome.To report SUSPECTED ADVERSE REACTIONS, contact Gland Pharma Limited at 866-770-7144 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

CLINICAL PHARMACOLOGY SECTION.

CLINICAL PHARMACOLOGY Pharmacokinetics The pharmacokinetics of foscarnet has been determined after administration as an intermittent intravenous infusion during induction therapy in AIDS patients with CMV retinitis. Observed plasma foscarnet concentrations in four studies (FOS-01, ACTG-015, FP48PK, FP49PK) are summarized in Table 7:TABLE Foscarnet Pharmacokinetic CharacteristicsValues expressed as mean S.D. (number of subjects studied) for each parameter Parameter60 mg/kg Q8h90 mg/kg Q12hC max at steady-state (uM)589 +- 192 (24)623 +- 132 (19)C trough at steady-state (uM)114 +- 91 (24)63 +- 57 (17)Volume of distribution (L/kg)0.41 +- 0.13 (12)0.52 +- 0.20 (18)Plasma half-life (hr)4.0 +- 2.0 (24)3.3 +- 1.4 (18)Systemic clearance (L/hr)6.2 +- 2.1 (24)7.1 +- 2.7 (18)Renal clearance (L/hr)5.6 +- 1.9 (5)6.4 +- 2.5 (13)CSF: plasma ratio0.69 +- 0.19 (9) 50 mg/kg Q8h for 28 days, samples taken hrs after end of hr infusion (Astra Report 815-04 AC025-1) 0.66 +- 0.11 (5) 90 mg/kg Q12hr for 28 days, samples taken hr after end of hr infusion (Hengge et al., 1993) Distribution In vitro studies have shown that 14 17% of foscarnet is protein bound at plasma drug concentrations of - 1000 uM.The foscarnet terminal half-life determined by urinary excretion was 87.5 +- 41.8 hours, possibly due to release of foscarnet from bone. Postmortem data on several patients in European clinical trials provide evidence that foscarnet does accumulate in bone in humans; however, the extent to which this occurs has not been determined.. Special Populations Adults with Impaired Renal Function: The pharmacokinetic properties of foscarnet have been determined in small group of adult subjects with normal and impaired renal function, as summarized in TABLE 8:TABLE Pharmacokinetic Parameters (mean +- S.D.) After Single 60 mg/kg Dose of foscarnet sodium Injection in GroupsGroup patients had normal renal function defined as creatinine clearance (CrCl) of >80 mL/min, Group CrCl was 50 80 mL/min, Group CrCl was 25 49 mL/min and Group CrCl was 10 24 mL/min. of Adults with Varying Degrees of Renal FunctionParameterGroup 1(N=6)Group 2(N=6)Group 3(N=6)Group 4(N=4)Creatinine clearance (mL/min)108 +- 1668 +- 834 +- 920 +- 4Foscarnet CL (mL/min/kg)2.13 +- 0.711.33 +- 0.430.46 +- 0.140.43 +- 0.26Foscarnet half-life (hr)1.93 +- 0.123.35 +- 0.8713.0 +- 4.0525.3 +- 18.7Total systemic clearance (CL) of foscarnet decreased and half-life increased with diminishing renal function (as expressed by creatinine clearance). Based on these observations, it is necessary to modify the dosage of foscarnet in patients with renal impairment (see DOSAGE AND ADMINISTRATION).. Drug Interaction The pharmacokinetics of foscarnet and ganciclovir were not altered in 13 patients receiving either concomitant therapy or daily alternating therapy for maintenance of CMV disease.There is no clinically significant interaction with zidovudine (AZT), or probenecid.. CLINICAL TRIALS CMV Retinitis A prospective, randomized, controlled clinical trial (FOS-03) was conducted in 24 patients with AIDS and CMV retinitis comparing treatment with foscarnet sodium Injection to no treatment. Patients received induction treatment of foscarnet sodium Injection, 60 mg/kg every hours for weeks, followed by maintenance treatment with 90 mg/kg/day until retinitis progression (appearance of new lesion or advancement of the border of posterior lesion greater than 750 microns in diameter). All diagnoses and determinations of retinitis progression were made from masked reading of retinal photographs. The 13 patients randomized to treatment with foscarnet sodium Injection had significant delay in progression of CMV retinitis compared to untreated controls. Median times to retinitis progression from study entry were 93 days (range 21 >364) and 22 days (range - 42), respectively.In another prospective clinical trial of CMV retinitis in patients with AIDS (ACTG-915), 33 patients were treated with two to three weeks of foscarnet sodium Injection induction (60 mg/kg TID) and then randomized to either 90 mg/kg/day or 120 mg/kg/day maintenance therapy. The median times from study entry to retinitis progression were not significantly different between the treatment groups, 96 (range 14 >176) days and 140 (range 16 >233) days, respectively.In study ACTG 129/FGCRT SOCA study 107 patients with newly diagnosed CMV retinitis were randomized to treatment with foscarnet sodium Injection (induction: 60 mg/kg TID for weeks; maintenance: 90 mg/kg QD) and 127 were randomized to treatment with ganciclovir (induction: mg/kg BID; maintenance: mg/kg QD). The median time to progression on the two drugs was similar (Fos=59 and Gcv=56 days).. Relapsed CMV Retinitis. The CMV Retinitis Retreatment Trial (ACTG 228/SOCA CRRT) was randomized, open- label comparison of foscarnet sodium Injection or ganciclovir monotherapy to the combination of both drugs for the treatment of persistently active or relapsed CMV retinitis in patients with AIDS. Subjects were randomized to one of the three treatments: Foscarnet sodium injection 90 mg/kg BID induction followed by 120 mg/kg QD maintenance (Fos); ganciclovir mg/kg BID induction followed by 10 mg/kg QD maintenance (Gcv); or the combination of the two drugs, consisting of continuation of the subjects current therapy and induction dosing of the other drug (as above), followed by maintenance with foscarnet sodium Injection 90 mg/kg QD plus ganciclovir mg/kg QD (Cmb). Assessment of retinitis progression was performed by masked evaluation of retinal photographs. The median times to retinitis progression or death were 39 days for the foscarnet sodium Injection group, 61 days for the ganciclovir group and 105 days for the combination group. For the alternative endpoint of retinitis progression (censoring on death), the median times were 39 days for the foscarnet sodium Injection group, 61 days for the ganciclovir group and 132 days for the combination group. Due to censoring on death, the latter analysis may overestimate the treatment effect. Treatment modifications due to toxicity were more common in the combination group than in the foscarnet sodium Injection or ganciclovir monotherapy groups (see ADVERSE REACTIONS section).. Mucocutaneous Acyclovir Resistant HSV Infections. In controlled trial, patients with AIDS and mucocutaneous, acyclovir-resistant HSV infection were randomized to either foscarnet sodium Injection (N=8) at dose of 40 mg/kg TID or vidarabine (N=6) at dose of 15 mg/kg per day. Eleven patients were nonrandomly assigned to receive treatment with foscarnet sodium Injection because of prior intolerance to vidarabine. Lesions in the eight patients randomized to foscarnet sodium Injection healed after 11 to 25 days; seven of the 11 patients nonrandomly treated with foscarnet sodium Injection healed their lesions in 10 to 30 days. Vidarabine was discontinued because of intolerance (N=4) or poor therapeutic response (N=2). In second trial, forty AIDS patients and three bone marrow transplant recipients with mucocutaneous, acyclovir-resistant HSV infections were randomized to receive foscarnet sodium Injection at dose of either 40 mg/kg BID or 40 mg/kg TID. Fifteen of the 43 patients had healing of their lesions in 11 to 72 days with no difference in response between the two treatment groups.

DOSAGE & ADMINISTRATION SECTION.

DOSAGE AND ADMINISTRATION CAUTION DO NOT ADMINISTER FOSCARNET SODIUM INJECTION BY RAPID OR BOLUS INTRAVENOUS INJECTION. THE TOXICITY OF FOSCARNET SODIUM INJECTION MAY BE INCREASED AS RESULT OF EXCESSIVE PLASMA LEVELS. CARE SHOULD BE TAKEN TO AVOID UNINTENTIONAL OVERDOSE BY CAREFULLY CONTROLLING THE RATE OF INFUSION. THEREFORE, AN INFUSION PUMP MUST BE USED. IN SPITE OF THE USE OF AN INFUSION PUMP, OVERDOSES HAVE OCCURRED.. ADMINISTRATION Instructions for Administration and Preparation. Foscarnet sodium injection is administered by controlled intravenous infusion, either by using central venous line or by using peripheral vein. The rate of infusion must be no more than mg/kg/minute. An individualized dose of foscarnet sodium Injection should be calculated on the basis of body weight (mg/kg), renal function, indication of use and dosing frequency (refer to DOSAGE subsection). To reduce the risk of nephrotoxicity, creatinine clearance (mL/min/kg) should be calculated even if serum creatinine is within the normal range, and doses should be adjusted accordingly. An individualized dose at the required concentration (24 mg/mL or 12 mg/mL) for the route of administration (central line or peripheral line) needs to be aseptically prepared prior to dispensing. The standard 24 mg/mL solution may be used with or without dilution when using central venous catheter for infusion. When peripheral vein catheter is used, the 24 mg/mL injection must be diluted to 12 mg/mL concentration with 5% dextrose in water or with normal saline solution prior to administration to avoid local irritation of peripheral veins. Dilutions and/or removals of excess quantities should be accomplished under aseptic conditions. Solutions thus prepared should be used within 24 hours of first entry into infusion bag.. Hydration. Hydration may reduce the risk of nephrotoxicity. Clinically dehydrated patients should have their condition corrected before initiating foscarnet sodium Injection therapy. It is recommended that 750 -1000 mL of normal saline or 5% dextrose solution should be given prior to the first infusion of foscarnet sodium Injection to establish diuresis. With subsequent infusions, 750 1000 mL of hydration fluid should be given with 90 120 mg/kg of foscarnet sodium Injection, and 500 mL with 40 60 mg/kg of foscarnet sodium Injection. Hydration fluid may need to be decreased if clinically warranted. Oral rehydration with similar regimens may be considered in certain patients.After the first dose, the hydration fluid should be administered concurrently with each infusion of foscarnet sodium Injection.. Compatibility With Other Solutions/Drugs. Other drugs and supplements can be administered to patient receiving foscarnet sodium Injection. However, care must be taken to ensure that foscarnet sodium Injection is only administered with normal saline or 5% dextrose solution and that no other drug or supplement is administered concurrently via the same catheter. Foscarnet has been reported to be chemically incompatible with 30% dextrose, amphotericin B, and solutions containing calcium such as Ringers lactate and TPN. Physical incompatibility with other IV drugs has also been reported including acyclovir sodium, ganciclovir, trimetrexate glucuronate, pentamidine isethionate, vancomycin, trimethoprim/sulfamethoxazole, diazepam, midazolam, digoxin, phenytoin, leucovorin, and proclorperazine. Because of foscarnets chelating properties, precipitate can potentially occur when divalent cations are administered concurrently in the same catheter.Parenteral drug products must be inspected visually for particulate matter and discoloration prior to administration whenever the solution and container permit. Solutions that are discolored or contain particulate matter should not be used.. Accidental Exposure. Accidental skin and eye contact with foscarnet sodium solution may cause local irritation and burning sensation. If accidental contact occurs, the exposed area should be flushed with water.. DOSAGE THE RECOMMENDED DOSAGE, FREQUENCY, OR INFUSION RATES SHOULD NOT BE EXCEEDED. ALL DOSES MUST BE INDIVIDUALIZED FOR PATIENTS RENAL FUNCTION.. Induction Treatment. The recommended initial dose of foscarnet sodium Injection for patients with normal renal function is:oFor CMV retinitis patients, either 90 mg/kg (1-1/2 to hour infusion) every twelve hours or 60 mg/kg (minimum one hour infusion) every eight hours over - weeks depending on clinical response.oFor acyclovir-resistant HSV patients, 40 mg/kg (minimum one hour infusion) either every or 12 hours for - weeks or until healed.An infusion pump must be used to control the rate of infusion. Adequate hydration is recommended to establish diuresis (see Hydration for recommendation), both prior to and during treatment to minimize renal toxicity (see WARNINGS), provided there are no clinical contraindications.. oFor CMV retinitis patients, either 90 mg/kg (1-1/2 to hour infusion) every twelve hours or 60 mg/kg (minimum one hour infusion) every eight hours over - weeks depending on clinical response.. oFor acyclovir-resistant HSV patients, 40 mg/kg (minimum one hour infusion) either every or 12 hours for - weeks or until healed.. Maintenance Treatment. Following induction treatment the recommended maintenance dose of foscarnet sodium Injection for CMV retinitis is 90 mg/kg/day to 120 mg/kg/day (individualized for renal function) given as an intravenous infusion over hours. Because the superiority of the 120 mg/kg/day has not been established in controlled trials, and given the likely relationship of higher plasma foscarnet levels to toxicity, it is recommended that most patients be started on maintenance treatment with dose of 90 mg/kg/day. Escalation to 120 mg/kg/day may be considered should early reinduction be required because of retinitis progression. Some patients who show excellent tolerance to foscarnet sodium Injection may benefit from initiation of maintenance treatment at 120 mg/kg/day earlier in their treatment.An infusion pump must be used to control the rate of infusion with all doses. Again, hydration to establish diuresis both prior to and during treatment is recommended to minimize renal toxicity, provided there are no clinical contraindications (see WARNINGS).Patients who experience progression of retinitis while receiving foscarnet sodium Injection maintenance therapy may be retreated with the induction and maintenance regimens given above or with combination of foscarnet sodium Injection and ganciclovir (see CLINICAL TRIALS section). Because of physical incompatibility, foscarnet sodium Injection and ganciclovir must NOT be mixed. Use in Patients with Abnormal Renal Function. Foscarnet sodium injection should be used with caution in patients with abnormal renal function because reduced plasma clearance of foscarnet will result in elevated plasma levels (see CLINICAL PHARMACOLOGY). In addition, foscarnet sodium Injection has the potential to further impair renal function (see WARNINGS). Safety and efficacy data for patients with baseline serum creatinine levels greater than 2.8 mg/dL or measured 24-hour creatinine clearances 50 mL/min are limited.Renal function must be monitored carefully at baseline and during induction and maintenance therapy with appropriate dose adjustments for foscarnet sodium Injection as outlined below (see Dose Adjustment and PATIENT MONITORING). During foscarnet sodium Injection therapy if creatinine clearance falls below the limits of the dosing nomograms (0.4 mL/min/kg), foscarnet sodium Injection should be discontinued, the patient hydrated, and monitored daily until resolution of renal impairment is ensured.Foscarnet sodium injection is not recommended in patients undergoing hemodialysis because dosage guidelines have not been established.. Dose Adjustment Foscarnet sodium injection dosing must be individualized according to the patients renal function status. Refer to TABLE 13 Foscarnet Sodium Injection Dosage Guide Induction below for recommended doses and adjust the dose as indicated. Even patients with serum creatinine in the normal range may require dose adjustment; therefore, the dose should be calculated at baseline and frequently thereafter.To use this dosing guide, actual 24-hour creatinine clearance (mL/min) must be divided by body weight (kg), or the estimated creatinine clearance in mL/min/kg can be calculated from serum creatinine (mg/dL) using the following formula (modified Cockcroft and Gault equation):TABLE 13 Foscarnet Sodium Injection Dosage Guide InductionHSV: Equivalent toCMV: Equivalent toCrCI(mL/min/kg)80 mg/kg/day total (40 mg/kg Q12h)120 mg/kg/day total(40 mg/kg Q8h)180 mg/kg/day total (60 mg/kg Q8h)(90 mg/kg Q12h)>1.440 Q12h40 Q8h60 Q8h90 Q12h>1.0 1.430 Q12h30 Q8h45 Q8h70 Q12h>0.8 1.020 Q12h35 Q12h50 Q12h50 Q12h>0.6 0.835 Q24h25 Q12h40 Q12h80 Q24h>0.5 0.625 Q24h40 Q24h60 Q24h60 Q24h>0.4 0.520 Q24h35 Q24h50 Q24h50 Q24h<0.4Not recommendedNot recommendedNot recommendedNot recommendedMaintenanceCMV: Equivalent toCrCI(mL/min/kg)90 mg/kg/day(once daily)120 mg/kg/day(once daily)>> means greater than, 1.490 Q24h120 Q24h>1.0 1.470 Q24h90 Q24h>0.8 1.050 Q24h65 Q24h>0.6 0.880 Q48h105 Q48h>0.5 0.660 Q48h80 Q48h>> means greater than or equal to, 0.4 0.550 Q48h65 Q48h<< means less than0.4Not recommendedNot recommended. (60 mg/kg Q8h)(90 mg/kg Q12h). Foscarnet Dosing Guide.

INFORMATION FOR PATIENTS SECTION.

Information for Patients CMV Retinitis: Patients should be advised that foscarnet sodium Injection is not cure for CMV retinitis, and that they may continue to experience progression of retinitis during or following treatment. They should be advised to have regular ophthalmologic examinations.Mucocutaneous Acyclovir-Resistant HSV Infections: Patients should be advised that foscarnet sodium Injection is not cure for HSV infections. While complete healing is possible, relapse occurs in most patients. Because relapse may be due to acyclovir-sensitive HSV, sensitivity testing of the viral isolate is advised. In addition, repeated treatment with foscarnet sodium Injection has led to the development of resistance associated with poorer response. In the case of poor therapeutic response, sensitivity testing of the viral isolate also is advised.Effects on Ability to Drive and Use Machines: Adverse effects such as dizziness and convulsions may occur during foscarnet sodium Injection therapy. Patients who experience seizures, dizziness, somnolence or other adverse reactions that could result in impairment, should be advised to avoid driving or operating machinery.General: Patients should be informed that the major toxicities of foscarnet are renal impairment, electrolyte disturbances, and seizures, and that dose modifications and possibly discontinuation may be required. The importance of close monitoring while on therapy must be emphasized. Patients should be advised of the importance of reporting to their physicians symptoms of perioral tingling, numbness in the extremities or paresthesias during or after infusion as possible symptoms of electrolyte abnormalities. Patients should also be advised to promptly report any cardiac symptoms. Should such symptoms occur, the infusion of foscarnet sodium Injection should be stopped, appropriate laboratory samples for assessment of electrolyte concentrations obtained, and physician consulted before resuming treatment. The rate of infusion must be no more than mg/kg/minute. The potential for renal impairment may be minimized by accompanying foscarnet sodium Injection administration with hydration adequate to establish and maintain diuresis during dosing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL Container LabelContainer LabelNDC 43066-089-10 250 mL FoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionRx only For Single Dose Only. Discard unused portion.Sterile, Nonpyrogenic, Preservative-free, PVC-free, DEHP-free.This container and container closure are not made with natural rubber latex.Each mL contains: 24 mg Foscarnet Sodium, USP, hydrochloric acid to adjust pH to 7.4 andWater for Injection, USP.Store at 20 to 25C (68 to 77F) [See USP Controlled Room Temperature.]Protect from excessive heat (above 40C) and from freezing. Use only if the infusion bag andtwist-off port stopper are intact, vacuum is present, and solution is clear and colorless.Do not remove bag from the overwrap until ready for use. Usual dosage: See package insert for dosage information. Administration Precautions: Administer by controlled intravenous infusion ata rate no more than mg/kg/minute. When administered via peripheral veincatheter, the 24 mg/mL injection must be diluted to 12 mg/mL concentration.Refer to package insert for compatible diluents and further instructions.Baxter LogoManufactured forBaxter Healthcare CorporationDeerfield, IL 60015 USAMade in IndiaCode No.: DRUGS/AP/01/2008LOTEXP(see above)1219000025GLFOS6000BUS07-34-00-1829Barcode3 43066 08910 8Carton LabelUn Varnish Area For Inner Shipper Label(Batch Details 2D Barcode)270 220 mmNDC 43066-089-10FoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)Barcode(01) 20343066089102For Single Dose Only. Discard unused portion.Sterile, Nonpyrogenic, Preservative-free, PVC-free, DEHP-free.This container and container closure are not made with natural rubber latex.Each mL contains: 24 mg Foscarnet Sodium, USP, hydrochloric acid to adjust pH to 7.4 andWater for Injection, USP.Store at 20 to 25C (68 to 77F). [See USP Controlled RoomTemperature.] Protect from excessive heat (above 40C) and fromfreezing. Use only if infusion bag and twist-off port stoppers areintact, vacuum is present, and solution is clear and colorless. Do notremove bag from the overwrap until ready for use.Usual dosage: See package insert for dosage information.Administration Precautions:Administer by controlled intravenous infusion at rate no more than1 mg/kg/minute. When administered via peripheral vein catheter,the 24 mg/mL injection must be diluted to 12 mg/mLconcentration.Refer to package insert for compatible diluents and furtherinstructions.Baxter LogoManufactured forBaxter Healthcare CorporationDeerfield, IL 60015 USAMade in India07-04-00-1021GLFOS6000BUSCode No.: DRUGS/AP/01/20081312001272-00NDC 43066-089-10 10 250 mL Single-Dose BagsFoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionBaxter LogoRx onlyNDC 43066-089-10 10 250 mL Single-Dose BagsFoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionBaxter LogoRx onlyNDC 43066-089-10 10 250 mL Single-Dose BagsFoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionBaxter LogoRx onlyOverpouch LabelNDC 43066-089-10 TO OPEN TEAR AT NOTCH250 mLFoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionRx onlyFor Single-Dose Only. Discard unused portion.Sterile, Nonpyrogenic, Preservative-free, PVC-free, DEHP-free.The container and container closure are not made with natural rubber latex.Each mL contains: 24 mg Foscarnet Sodium, USP, hydrochloric acid to adjustpH to 7.4 and Water for Injection, USP.Store at 20 to 25C (68 to 77F). [See USP Controlled Room Temperature.] Protect fromexcessive heat (above 40C) and from freezing. Use only if infusion bag and twist-off portstoppers are intact, vacuum is present, and solution is clear and colorless. Do not removebag from the overwrap until ready for use.Usual dosage: See package insert for dosage information.Administration Precautions:Administer by controlled intravenous infusion at rate no more than mg/kg/minute.When administered via peripheral vein catheter, the 24 mg/mL injection must bediluted to 12 mg/mL concentration.Refer to package insert for compatible diluents and further instructions.Baxter LogoGLFOS6000BUS07-07-00-1912Code No.: DRUGS/AP/01/20081311001201-00LOT:EXP:Un varnish area forBatch details (To be printedonline) 50 28 mmBarcode3 43066 08910 8NDC 43066-089-10 Rx onlyFoscarnetSodium Injection6,000 mg per 250 mL(24 mg per mL)For Central Intravenous Infusion OnlyMust Be Diluted for Peripheral Intravenous InfusionBaxter Logo07-07-00-1913Code No.: DRUGS/AP/01/20081311001202-00Barcode3 43066 08910 8. Foscarnet Container Label 43066-089-10. Foscarnet Carton Label 43066-089-10 of 3. Foscarnet Carton Label 43066-089-10 of 3. Foscarnet Carton Label 43066-089-10 of 3. Foscarnet Overpouch Label 43066-089-10 of 2. Foscarnet Overpouch Label 43066-089-10 of 2.

PRECAUTIONS SECTION.

PRECAUTIONS General Care must be taken to infuse solutions containing foscarnet sodium Injection only into veins with adequate blood flow to permit rapid dilution and distribution to avoid local irritation (see DOSAGE AND ADMINISTRATION). Local irritation and ulcerations of penile epithelium have been reported in male patients receiving foscarnet sodium Injection, possibly related to the presence of drug in the urine. Cases of male and female genital irritation/ulceration have been reported in patients receiving foscarnet sodium Injection. Adequate hydration with close attention to personal hygiene may minimize the occurrence of such events.Due to the sodium content of foscarnet sodium Injection (240 micromoles (5.5 mg) of sodium per mL), avoid foscarnet sodium Injection use when intravenous infusion of large amount of sodium or water may not be tolerated (e.g. in patients with cardiomyopathy). Foscarnet sodium injection should also be avoided in patients on controlled sodium diet.. Hematopoietic System Anemia has been reported in 33% of patients receiving foscarnet sodium Injection in controlled studies. Granulocytopenia has been reported in 17% of patients receiving foscarnet sodium Injection in controlled studies; however, only 1% (2/189) were terminated from these studies because of neutropenia.. Information for Patients CMV Retinitis: Patients should be advised that foscarnet sodium Injection is not cure for CMV retinitis, and that they may continue to experience progression of retinitis during or following treatment. They should be advised to have regular ophthalmologic examinations.Mucocutaneous Acyclovir-Resistant HSV Infections: Patients should be advised that foscarnet sodium Injection is not cure for HSV infections. While complete healing is possible, relapse occurs in most patients. Because relapse may be due to acyclovir-sensitive HSV, sensitivity testing of the viral isolate is advised. In addition, repeated treatment with foscarnet sodium Injection has led to the development of resistance associated with poorer response. In the case of poor therapeutic response, sensitivity testing of the viral isolate also is advised.Effects on Ability to Drive and Use Machines: Adverse effects such as dizziness and convulsions may occur during foscarnet sodium Injection therapy. Patients who experience seizures, dizziness, somnolence or other adverse reactions that could result in impairment, should be advised to avoid driving or operating machinery.General: Patients should be informed that the major toxicities of foscarnet are renal impairment, electrolyte disturbances, and seizures, and that dose modifications and possibly discontinuation may be required. The importance of close monitoring while on therapy must be emphasized. Patients should be advised of the importance of reporting to their physicians symptoms of perioral tingling, numbness in the extremities or paresthesias during or after infusion as possible symptoms of electrolyte abnormalities. Patients should also be advised to promptly report any cardiac symptoms. Should such symptoms occur, the infusion of foscarnet sodium Injection should be stopped, appropriate laboratory samples for assessment of electrolyte concentrations obtained, and physician consulted before resuming treatment. The rate of infusion must be no more than mg/kg/minute. The potential for renal impairment may be minimized by accompanying foscarnet sodium Injection administration with hydration adequate to establish and maintain diuresis during dosing.. Drug Interactions A possible drug interaction of foscarnet sodium Injection and intravenous pentamidine has been described. Concomitant treatment of four patients in the United Kingdom with foscarnet sodium Injection and intravenous pentamidine may have caused hypocalcemia; one patient died with severe hypocalcemia. Toxicity associated with concomitant use of aerosolized pentamidine has not been reported. Because foscarnet sodium Injection can reduce serum levels of ionized calcium, extreme caution is advised when used concurrently with other drugs known to influence serum calcium levels (e.g., intravenous pentamidine). Renal impairment and symptomatic hypocalcemia have been observed during concurrent treatment with foscarnet sodium Injection and intravenous pentamidine.Because of foscarnets tendency to cause renal impairment, the use of foscarnet sodium Injection should be avoided in combination with potentially nephrotoxic drugs such as aminoglycosides, amphotericin B, cyclosporine, acyclovir, methotrexate, tacrolimus and intravenous pentamidine (see above) unless the potential benefits outweigh the risks to the patient.When diuretics are indicated, thiazides are recommended over loop diuretics because the latter inhibit renal tubular secretion, and may impair elimination of foscarnet sodium Injection, potentially leading to toxicity.Abnormal renal function has been observed in clinical practice during the use of foscarnet sodium Injection and ritonavir, or foscarnet sodium Injection, ritonavir, and saquinavir. (See DOSAGE and ADMINISTRATION.)Because of the risk of QT prolongation and the potential for torsades de pointes, the use of foscarnet sodium Injection should be avoided in combination with agents known to prolong the QT interval including Class IA (e.g., quinidine or procainamide) or Class III (e.g., dofetilide, amiodarone, sotalol) antiarrhythmic agents, phenothiazines, tricyclic antidepressants, and certain macrolides and fluoroquinolones.. Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenicity studies were conducted in rats and mice at oral doses of 500 mg/kg/day and 250 mg/kg/day. Oral bioavailability in unfasted rodents is 20%. No evidence of oncogenicity was reported at plasma drug levels equal to 1/3 and 1/5, respectively, of those in humans (at the maximum recommended human daily dose) as measured by the area-under-the-time/concentration curve (AUC).Foscarnet sodium injection showed genotoxic effects in the BALB/3T3 in vitro transformation assay at concentrations greater than 0.5 mcg/mL and an increased frequency of chromosome aberrations in the sister chromatid exchange assay at 1000 mcg/mL. high dose of foscarnet (350 mg/kg) caused an increase in micronucleated polychromatic erythrocytes in vivo in mice at doses that produced exposures (area under curve) comparable to that anticipated clinically.. Pregnancy. There are no adequate and well-controlled studies of foscarnet sodium Injection in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.Animal Data: Foscarnet sodium injection did not adversely affect fertility and general reproductive performance in rats. The results of peri- and post-natal studies in rats were also negative. However, these studies used exposures that are inadequate to define the potential for impairment of fertility at human drug exposure levels.Daily subcutaneous doses up to 75 mg/kg administered to female rats prior to and during mating, during gestation, and 21 days post-partum caused slight increase (< 5%) in the number of skeletal anomalies compared with the control group. Daily subcutaneous doses up to 75 mg/kg administered to rabbits and 150 mg/kg administered to rats during gestation caused an increase in the frequency of skeletal anomalies/variations. On the basis of estimated drug exposure (as measured by AUC), the 150 mg/kg dose in rats and 75 mg/kg dose in rabbits were approximately one-eighth (rat) and one-third (rabbit) the estimated maximal daily human exposure. These studies are inadequate to define the potential teratogenicity at levels to which women will be exposed.. Nursing Mothers. It is not known whether foscarnet sodium Injection is excreted in human milk; however, in lactating rats administered 75 mg/kg, foscarnet sodium Injection was excreted in maternal milk at concentrations three times higher than peak maternal blood concentrations. Because of the potential for serious adverse events in nursing infants, decision should be made whether to discontinue nursing or discontinue drug, taking into consideration the importance of the drug to the mother. The Centers for Disease Control and Prevention recommend that HIV-infected mothers not breast- feed their infants to avoid risking postnatal transmission of HIV.. Pediatric Use The safety and effectiveness of foscarnet sodium Injection in pediatric patients have not been established. Foscarnet sodium injection is deposited in teeth and bone and deposition is greater in young and growing animals. Foscarnet sodium injection has been demonstrated to adversely affect development of tooth enamel in mice and rats. The effects of this deposition on skeletal development have not been studied.Since deposition in human bone has also been shown to occur, it is likely that it does so to greater degree in developing bone in pediatric patients. Administration to pediatric patients should be undertaken only after careful evaluation and only if the potential benefits for treatment outweigh the risks.. Geriatric Use No studies of the efficacy or safety of foscarnet sodium Injection in persons 65 years of age or older have been conducted. However, foscarnet sodium Injection has been used in patients age 65 years of age and older. The pattern of adverse events seen in these patients is consistent across all age groups. This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and renal function should be monitored. (See DOSAGE AND ADMINISTRATION).

SPL UNCLASSIFIED SECTION.

VIROLOGY Mechanism of Action Foscarnet exerts its antiviral activity by selective inhibition at the pyrophosphate binding site on virus-specific DNA polymerases at concentrations that do not affect cellular DNA polymerases. Foscarnet does not require activation (phosphorylation) by thymidine kinase or other kinases.. Antiviral Activity in Cell Culture The quantitative relationship between the cell culture susceptibility of human cytomegalovirus (CMV) or herpes simplex virus and (HSV-1 and HSV-2) to foscarnet and clinical response to therapy has not been established and virus sensitivity testing has not been standardized. Sensitivity test results, expressed as the concentration of drug required to inhibit by 50% the growth of virus in cell culture (EC50), vary greatly depending on the assay method used, cell type employed and the laboratory performing the test. number of sensitive viruses and their EC50 values are listed below (TABLE 1). The combination antiviral activity of foscarnet and ganciclovir or acyclovir are not antagonistic in cell culture.TABLE Foscarnet Inhibition of Virus Replication in Cell CultureVirusEC50 value (uM)CMVGanciclovir resistant CMVHSV-1, HSV-2HSV-TK negative mutantHSV-DNA polymerase mutants50 800Mean 269 uM 19010 -130675 443. Antiviral Activity in vivo Statistically significant decreases in positive CMV cultures from blood and urine have been demonstrated in two studies (FOS-03 and ACTG-015/915) of subjects treated with foscarnet sodium Injection. Although median time to progression of CMV retinitis was increased in subjects treated with foscarnet sodium Injection, reductions in positive blood or urine cultures have not been shown to correlate with clinical efficacy in individual subjects (TABLE 2).TABLE Blood and Urine Culture Results from CMV Retinitis PatientsA total of 77 subjects were treated with foscarnet sodium Injection in two clinical trials (FOS-03 and ACTG-015/915). Not all subjects had blood or urine cultures done and some subjects had results from both cultures.+(60 mg/kg foscarnet sodium Injection TID for 2-3 weeks). Blood+CMV-CMVBaselineEnd of Induction+2713460Urine+CMV-CMVBaselineEnd of Induction+5221637. Resistance Cell culture: CMV and HSV isolates with reduced susceptibility to foscarnet have been selected in cell culture by passage of wild type virus in the presence of increasing concentrations of the drug. All foscarnet resistant isolates are known to be generated through amino acid substitutions in the viral DNA polymerase pUL54 (CMV) or pUL30 (HSV) (TABLE 3).TABLE Summary of Foscarnet Resistance-associated DNA Polymerase Amino Acid Substitutions in Cell Culture CMVpUL54T419M, T552N, S585A, F595I, Q807A, M844T/V, V946LHSV-1pUL30Y577H, E597D, A605V, L702H, V714M, L774F, L788M, D780N, L782I, P797T, L802F, V813M, V817M, Y818C, T821M, R842S, S889A, F891C, V892M, D907V, A910V, SRA914-916LCV, V958L, R959HHSV-2pUL30In vivo: Limited clinical data are available on the development of clinical resistance to foscarnet and many pathways to resistance likely exist. Substitutions documented in the literature in treated patients as associated with foscarnet resistance, are listed in TABLE 4.TABLE Summary of Foscarnet Resistance-associated Amino Acid Substitutions Observed in Treated PatientsCMV pUL54N495K, Q578H/L, D588E/N, T700A, V715M, E756D/K/Q, L773V, L776M, V781I, V787L, L802M, A809V, V812L, T813S, T821I, A834P,T838A, G841A/S, del 981-982HSV-1pUL30S599L, D672N, R700G, V715G, A719T/V, S724N, E798K, G841C/S,A910T, Y941HHSV-2pUL30A724T, S725G, S729N, Q732R, L783M, D785N, T844I, L850I, D912VNote: Many additional pathways to foscarnet resistance likely existThe possibility of viral resistance should be considered in patients who show poor clinical response or experience persistent viral excretion during therapy.Cross-Resistance: The amino acid substitutions that resulted in reduced susceptibility to foscarnet and either ganciclovir, acyclovir and/or cidofovir are summarized in Tables and 6.TABLE Summary of CMV DNA polymerase Amino Acid Substitutions Conferring Foscarnet Resistance with Cross-Resistance to Ganciclovir and/or CidofovirCross-resistant to ganciclovirCMV pUL54Q578H, D588N, E756K, L773V, L776M, V781I, V787L, L802M, A809V, V812L, T813S, T821I, A834P, G841A/S, del 981-982Cross-resistant tocidofovirCMVpUL54Q578H, D588N, E756K, L773V, V812L, T813S, A834P, G841A, del 981-982TABLE Summary of HSV DNA polymerase Amino Acid Substitutions Conferring Foscarnet Resistance with Cross-Resistance to Acyclovir and/or CidofovirCross-resistant to acyclovirHSV-1 pUL30E597D, S599L, A605V, D672N, R700G, L702H, V714M, V715G, A719T/V, S724N, L774F, L778M, D780N, L782I, P797T, E798K, L802F, V813M, V817M, Y818C, T821M, G841C/S, R842S, S889A, F891C/Y, V892M, D907V, A910V/T, SRA914-916LCV, Y941H, V958L, V959HHSV-2pUL30A724T, S725G, S729N, Q732R, L783M, D785N, T844I, D912VMarginally cross-resistant to cidofovirHSV-1pUL30V714M, A719V, S724N, L778M, L802F, Y818C, T821M, G841SHSV-2pUL30L783M.

WARNINGS SECTION.

WARNINGS Renal Impairment THE MAJOR TOXICITY OF FOSCARNET SODIUM INJECTION IS RENAL IMPAIRMENT (see ADVERSE REACTIONS section). Renal impairment is most likely to become clinically evident during the second week of induction therapy, but may occur at any time during foscarnet sodium Injection treatment. Renal function should be monitored carefully during both induction and maintenance therapy (see PATIENT MONITORING section). Elevations in serum creatinine are usually, but not always, reversible following discontinuation or dose adjustment of foscarnet sodium Injection. Safety and efficacy data for patients with baseline serum creatinine levels greater than 2.8 mg/dL or measured 24-hour creatinine clearances <50 mL/min are limited.SINCE FOSCARNET SODIUM INJECTION HAS THE POTENTIAL TO CAUSE RENAL IMPAIRMENT, DOSE ADJUSTMENT BASED ON SERUM CREATININE IS NECESSARY. Hydration may reduce the risk of nephrotoxicity. It is recommended that 750 1000 mL of normal saline or 5% dextrose solution should be given prior to the first infusion of foscarnet sodium Injection to establish diuresis. With subsequent infusions, 750 1000 mL of hydration fluid should be given with 90 120 mg/kg of foscarnet sodium Injection, and 500 mL with 40 60 mg/kg of foscarnet sodium Injection. Hydration fluid may need to be decreased if clinically warranted.After the first dose, the hydration fluid should be administered concurrently with each infusion of foscarnet sodium Injection.. Mineral and Electrolyte Abnormalities Foscarnet sodium injection has been associated with changes in serum electrolytes including hypocalcemia, hypophosphatemia, hyperphosphatemia, hypomagnesemia, and hypokalemia (see ADVERSE REACTIONS section). Foscarnet sodium injection may also be associated with dose-related decrease in ionized serum calcium which may not be reflected in total serum calcium. This effect is likely to be related to chelation of divalent metal ions such as calcium by foscarnet. Patients should be advised to report symptoms of low ionized calcium such as perioral tingling, numbness in the extremities and paresthesias. Particular caution and careful management of serum electrolytes is advised in patients with altered calcium or other electrolyte levels before treatment and especially in those with neurologic or cardiac abnormalities and those receiving other drugs known to influence minerals and electrolytes (see PATIENT MONITORING and Drug Interactions sections). Physicians should be prepared to treat these abnormalities and their sequelae such as tetany, seizures or cardiac disturbances. The rate of foscarnet sodium Injection infusion may also affect the decrease in ionized calcium. Therefore, an infusion pump must be used for administration to prevent rapid intravenous infusion (see DOSAGE AND ADMINISTRATION section). Slowing the infusion rate may decrease or prevent symptoms.. Seizures Seizures related to mineral and electrolyte abnormalities have been associated with foscarnet sodium Injection treatment (see WARNING section; Mineral and Electrolyte Abnormalities). Several cases of seizures were associated with death. Cases of status epilepticus have been reported. Risk factors associated with seizures included impaired baseline renal function, low total serum calcium, and underlying CNS conditions.. Hypersensitivity Serious acute hypersensitivity reactions (e.g., anaphylactic shock, urticaria, angioedema) have been reported postmarketing in patients receiving foscarnet sodium Injection (see ADVERSE REACTIONS section). If such an acute reaction occurs, therapy should be discontinued and appropriate medical therapy immediately instituted.. QT prolongation and torsade de pointes Foscarnet sodium injection has been associated with prolongation of the QT interval, an ECG abnormality that has been associated with torsades de pointes, which has been reported during postmarketing surveillance for foscarnet sodium Injection (see ADVERSE REACTIONS section). Some of these patients had confounding risk factors such as underlying cardiac disease, electrolyte abnormalities and other concomitant medications.Use with caution in patients who have history of QT prolongation, in patients who are taking medications known to prolong the QT interval (see PRECAUTIONS section), in patients with electrolyte disturbances, or in patients who have other risk factors for QT prolongation. Electrocardiograms (ECGs) and measurement of electrolytes should be obtained prior to treatment initiation and periodically during treatment with foscarnet sodium Injection.