Phendimetrazine Tartrate
Pronouncation: (fen-dye-ME-tra-zeen TAR-trate)Class: Anorexiant
Trade Names:
Bontril PDM
- Tablets 35 mg
Trade Names:
Bontril Slow-Release
- Tablets 35 mg
Trade Names:
Melfiat-105 Unicelles
- Tablets 35 mg
Trade Names:
Prelu-2
- Capsules, sustained-release 105 mg
Pharmacology
May stimulate satiety center in brain, causing appetite suppression.
Pharmacokinetics
Absorption
Phendimetrazine is readily absorbed.
Metabolism
Phendimetrazine metabolism is hepatic. Some of the drug is metabolized to phenmetrazine and phendimetrazine-N-oxide.
Elimination
Excretion is via the kidneys and is increased by acidifying the urine. The t ½ is 1.9 h (immediate-release) and 9.8 h (slow-release).
Duration
4 hr.
Indications and Usage
Short-term (few weeks) adjunct to diet plan to reduce weight.
Contraindications
Hypersensitivity to sympathomimetic amines; pregnancy; advanced arteriosclerosis; symptomatic CV disease; moderate to severe hypertension; hyperthyroidism; glaucoma; agitated states; history of drug abuse; during or within 14 days following the administration of an MAOI.
Dosage and Administration
Adults and children (12 yr of age or older)PO Tablets or capsules: 35 mg 2 or 3 times daily before meals; sustained-release capsules: 105 mg once daily in the morning before breakfast.
General Advice
Swallow sustained-release capsule whole. Do not crush, chew, or open capsule.
Storage/Stability
Store at controlled room temperature (59° to 86°F).
Drug Interactions
GuanethidineMay decrease hypotensive effect of guanethidine.
MAOIs (eg, phenelzine); furazolidoneMay cause hypertensive crisis and intracranial hemorrhage.
Selective serotonin reuptake inhibitors (eg, fluoxetine)Sympathomimetic effects of phendimetrazine and risk of “serotonin syndrome” may be increased.
Laboratory Test Interactions
None well documented.
Adverse Reactions
Cardiovascular
Palpitation; tachycardia, hypertension.
CNS
Overstimulation; restlessness; dizziness; insomnia; euphoria; dysphoria; tremor; headache; psychosis.
Dermatologic
Allergic urticaria.
GI
Dry mouth; unpleasant taste; diarrhea; constipation.
Genitourinary
Impotence; changes in libido.
Precautions
Pregnancy
Do not use in women who are pregnant or may become pregnant.
Lactation
Undetermined.
Children
Safety and efficacy not established in children younger than 12 yr of age.
Special Risk Patients
Use with caution in patients with glaucoma, hypertension, diabetes mellitus.
Drug dependence
Psychological and physical dependence may occur with continued use; this class of drugs has been extensively abused.
Tolerance
Tolerance to the anorectic effect usually develops within a few weeks.
Overdosage
Symptoms
Restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, panic states, fatigue, depression, arrhythmias, hypertension, hypotension, circulatory collapse, nausea, vomiting, diarrhea, abdominal cramps, convulsions, coma, death.
Patient Information
- Advise patient using immediate-release tablet to take prescribed dose 1 h before meals and to take last dose several hours before bedtime.
- Advise patient using sustained-release capsule that medication is slowly released over 12 h and to take dose in the morning. Advise patient to swallow the capsule whole and to not crush or chew the capsule.
- Encourage patient to follow medically supervised weight reduction program. Emphasize that this medication will only work in conjunction with a caloric restricted diet and exercise program.
- Advise patient that medication should be taken as prescribed and to not stop taking or change the dose unless advised to do so by the health care provider.
- Explain that appetite suppressant effects are temporary and tolerance to medication and dependence can occur. Caution patient not to increase the dose in an effort to overcome the tolerance when it occurs.
- Remind diabetic patient to monitor blood sugar more frequently while implementing dietary restrictions and to notify health care provider if significant changes in blood sugar occur.
- Caution patient that drug may impair the ability to drive or perform other tasks requiring mental alertness.
- Advise patient to notify health care provider immediately if the following symptoms occur: chest pain, palpitations, nervousness, dizziness.
- Advise patient to notify health care provider if experiencing any unusual or unexplained symptoms.
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