DOSAGE & ADMINISTRATION SECTION.
DOSAGE ADMINISTRATION. Usual Adult Dose: tablet (35 mg) b.i.d. or t.i.d., one hour before meals.Dosage should be individualized to obtain an adequate response with the lowest effective dosage. In some cases, 1/2 tablet (17.5 mg) per dose may be adequate. Dosage should not exceed tablets t.i.d.
ADVERSE REACTIONS SECTION.
ADVERSE REACTIONS. Cardiovascular: Palpitation, tachycardia, elevated blood pressure.Central Nervous System: Overstimulation, restlessness, insomnia, agitation, flushing, tremor, sweating, dizziness, headache, psychotic state, blurring of vision.Gastrointestinal: Dryness of the mouth, nausea, diarrhea, constipation, stomach pain.Genitourinary: Urinary frequency, dysuria, changes in libido.
CLINICAL PHARMACOLOGY SECTION.
CLINICAL PHARMACOLOGY. Phendimetrazine tartrate is phenylalkylamine sympathomimetic amine with pharmacological activity similar to the prototype drugs of this class used in obesity, the amphetamines. Actions include central nervous system stimulation and elevation of blood pressure. Tachyphylaxis and tolerance have been demonstrated with all drugs of this class in which these phenomena have been looked for.Drugs of this class used in obesity are commonly known as anorectics or anorexigenics. It has not been established, however, that the action of such drugs in treating obesity is primarily one of appetite suppression. Other central nervous system actions or metabolic effects, may be involved, for example.Adult obese subjects instructed in dietary management and treated with anorectic drugs, lose more weight on the average than those treated with placebo and diet, as determined in relatively short term clinical trials.The magnitude of increased weight loss of drug-treated patients over placebo-treated patients is only fraction of pound week. The rate of weight loss is greatest in the first weeks of therapy for both drug and placebo subjects and tends to decrease in succeeding weeks. The possible origins of the increased weight loss due to the various drug effects are not established. The amount of weight loss associated with the use of an anorectic drug varies from trial to trial, and the increased weight loss appears to be related in part to variables other than the drug prescribed, such as the physician investigator, the population treated, and the diet prescribed. Studies do not permit conclusions as to the relative importance of the drug and non-drug factors on weight loss.The natural history of obesity is measured in years, whereas the studies cited are restricted to few weeks duration, thus, the total impact of drug-induced weight loss over that of diet alone must be considered clinically limited.
CONTRAINDICATIONS. Known hypersensitivity or idiosyncratic reactions to sympathomimetics.Advanced arteriosclerosis, symptomatic cardiovascular disease, moderate and severe hypertension, hyperthyroidism, and glaucoma.Highly nervous or agitated patients.Patients with history of drug abuse.Patients taking other CNS stimulants, including monoamine oxidase inhibitors.
DESCRIPTION Phendimetrazine tartrate, as the dextro isomer, has the chemical name of (2S, 3S)-3, 4-Dimethyl-2-phenylmorpholine L-(+)-tartrate (1:1).Phendimetrazine tartrate is white, odorless crystalline powder. It is freely soluble in water; sparingly soluble in warm alcohol, insoluble in chloroform, acetone, ether and benzene.Each tablet, for oral administration, contains 35 mg of phendimetrazine tartrate. In addition, each tablet contains the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, magnesium stearate, microcrystalline cellulose and FD and Blue Lake or FD and Yellow and and Yellow 10 as coloring.
DRUG ABUSE AND DEPENDENCE SECTION.
DRUG ABUSE AND DEPENDENCE. Controlled Substance Phendimetrazine tartrate tablets are defined by the Drug Enforcement Administration as Schedule III controlled substance.Dependence Phendimetrazine tartrate is related chemically and pharmacologically to the amphetamines. Amphetamines and related stimulant drugs have been extensively abused, and the possibility of abuse of phendimetrazine should be kept in mind when evaluating the desirability of including drug as part of weight reduction program. Abuse of amphetamines and related drugs may be associated with intense psychological dependence and severe social dysfunction. There are reports of patients who have increased the dosage to many times that recommended. Abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression; changes are also noted on the sleep EEG. Manifestations of chronic intoxication with anorectic drugs include severe dermatoses, marked insomnia, irritability, hyperactivity and personality changes. The most severe manifestation of chronic intoxications is psychosis, often clinically indistinguishable from schizophrenia.
HOW SUPPLIED SECTION.
HOW SUPPLIED. Each single-scored, yellow, round tablet contains 35 mg phendimetrazine tartrate. Tablets are supplied as follows:NDC NBR. TABLETS PER BOTTLE21695-597-07 721695-597-21 2121695-597-42 4221695-597-60 60Store at controlled room temperature 15o-30oC (59o-86oF).Dispense in tight containers with child-resistant closures.Distributed By: Bryant Ranch Prepack12623 Sherman Way North Hollywood, CA 91605 Voice (877) 885-0882 Fax (877) 277-7552Repackaged by:Rebel Distributors CorpThousand Oaks, CA 91320.
OVERDOSAGE. Acute overdosage with phendimetrazine tartrate may manifest itself by the following signs and symptoms: unusual restlessness, confusion, belligerence, hallucinations, and panic states. Fatigue and depression usually follow the central stimulation. Cardiovascular effects include arrhythmias, hypertension, or hypotension and circulatory collapse. Gastrointestinal symptoms include nausea, vomiting, diarrhea, and abdominal cramps. Poisoning may result in convulsions, coma, and death.The management of overdosage is largely symptomatic. It includes sedation with barbiturate. If hypertension is marked, the use of nitrate or rapid-acting alpha receptor-blocking agent should be considered. Experience with hemodialysis or peritoneal dialysis is inadequate to permit recommendations for its use.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.
Principal Display Panel. Phendimetrazine Tartrate 35mg.
PRECAUTIONS Caution is to be exercised in prescribing phendimetrazine tartrate for patients with even mild hypertension.Insulin requirements in diabetes mellitus may be altered in association with the use of phendimetrazine and the concomitant dietary regimen.Phendimetrazine may decrease the hypotensive effect of guanethidine.The least amount feasible should be prescribed or dispensed at one time in order to minimize the possibility of overdosage.Usage in Pregnancy Safe use in pregnancy has not been established. Until more information is available, phendimetrazine tartrate should not be taken by women who are or may become pregnant unless, in the opinion of the physician, the potential benefits outweigh the possible hazards.Pediatric Patients Phendimetrazine tartrate is not recommended for use in pediatric patients under 12 years of age.