Dosage Form: tablet
Medically reviewed by Drugs.com. Last updated on Sep 23, 2019.
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Reserpine, USP is an antihypertensive, available as 0.1 mg and 0.25 mg tablets for oral administration. Its chemical name is methyl 18β-hydroxy-11,17 α-dimethoxy-3β, 20α-yohimban-16β-carboxylate 3,4,5-trimethoxybenzoate (ester) and its structural formula is:
Reserpine USP, a pure crystalline alkaloid of rauwolfia, is a white or pale buff to slightly yellowish, odorless crystalline powder. It darkens slowly on exposure to light, but more rapidly when in solution. It is insoluble in water, freely soluble in acetic acid and in chloroform, slightly soluble in benzene, and very slightly soluble in alcohol and in ether. Its molecular weight is 608.69.
Inactive Ingredients: Acacia, confectioner’s sugar1, corn starch, lactose monohydrate, magnesium stearate.
This product complies with Dissolution Test #2.
In 0.25 mg tablets only.
Reserpine - Clinical Pharmacology
Reserpine depletes stores of catecholamines and 5-hydroxytryptamine in many organs, including the brain and adrenal medulla. Most of its pharmacological effects have been attributed to this action. Depletion is slower and less complete in the adrenal medulla than in other tissues. The depression of sympathetic nerve function results in a decreased heart rate and a lowering of arterial blood pressure. The sedative and tranquilizing properties of Reserpine are thought to be related to depletion of catecholamines and 5-hydroxytryptamine from the brain.
Reserpine, like other rauwolfia compounds, is characterized by slow onset of action and sustained effects. Both cardiovascular and central nervous system effects may persist for a period of time following withdrawal of the drug.
Mean maximum plasma levels of plasma concentrations after a single dose of 0.5 mg of Reserpine, administered as two 0.25 mg tablets or as an aqueous solution, peaked after 2.5 hours. The mean peak level was approximately 1.1 ng/ml. The two formulations were found to be bioequivalent. Absolute bioavailability of Reserpine, as established by comparison to an intravenous dose, has been reported to be approximately 50%.
Reserpine is extensively bound (95%) to plasma proteins. Reserpine is almost completely metabolized in the body, and only about 1% is excreted as unchanged drug in the urine. No definitive studies on the human metabolism of Reserpine have been made. After oral administration, an initial half-life of approximately 5 hours is followed by a terminal half-life of the order of 200 hours. Plasma levels may be measurable 14 days after a single dose. The clinical significance of the long terminal half-life is unknown.
Indications and Usage for Reserpine
Mild essential hypertension; also useful as adjunctive therapy with other antihypertensive agents in the more severe forms of hypertension; relief of symptoms in agitated psychotic states (e.g., schizophrenia), primarily in those individuals unable to tolerate phenothiazine derivatives or in those who also require antihypertensive medication.
Known hypersensitivity, mental depression or history of mental depression (especially with suicidal tendencies), active peptic ulcer, ulcerative colitis, and patients receiving electroconvulsive therapy.
Extreme caution should be exercised in treating patients with a history of mental depression. Reserpine may cause mental depression. Recognition of depression may be difficult because this condition may often be disguised by somatic complaints (Masked Depression). The drug should be discontinued at first signs of depression such as despondency, early morning insomnia, loss of appetite, impotence, or self-deprecation. Drug-induced depression may persist for several months after drug withdrawal and may be severe enough to result in suicide.
Since Reserpine increases gastrointestinal motility and secretion, it should be used cautiously in patients with a history of peptic ulcer, ulcerative colitis, or gallstones (biliary colic may be precipitated).
Caution should be exercised when treating hypertensive patients with renal insufficiency, since they adjust poorly to lowered blood pressure levels.
Preoperative withdrawal of Reserpine does not assure that circulatory instability will not occur. It is important that the anesthesiologist be aware of the patient’s drug intake and consider this in the overall management, since hypotension has occurred in patients receiving rauwolfia preparations. Anticholinergic and/or adrenergic drugs (e.g., metaraminol, norepinephrine) have been employed to treat adverse vagocirculatory effects.
Information for Patients
Patients should be informed of possible side effects and advised to take the medication regularly and continuously as directed.
MAO inhibitors should be avoided or used with extreme caution.
Concurrent use of tricyclic antidepressants may decrease the antihypertensive effect of Reserpine.
Concurrent use of Reserpine and direct-or-indirect acting sympathomimetics should be closely monitored. The action of direct-acting amines (epinephrine, isoproterenol, phenylephrine, metaraminol) may be prolonged when given to patients taking Reserpine. The action of indirect-acting amines (ephedrine, tyramine, amphetamines) is inhibited.
Reserpine should be used cautiously with digitalis and quinidine, since cardiac arrhythmias have occurred with rauwolfia preparations.
Concomitant use of Reserpine with other antihypertensive agents necessitates careful titration of dosage with each agent.
Carcinogenesis, Mutagenesis, Impairment of FertilityAnimal Tumorigenicity
Rodent studies have shown that Reserpine is an animal tumorigen, causing an increased incidence of mammary fibroadenomas in female mice, malignant tumors of the seminal vesicles in male mice, and malignant adrenal medullary tumors in male rats. These findings arose in 2-year studies in which the drug was administered in the feed at concentrations of 5 to 10 ppm – about 100 to 300 times the usual human dose. The breast neoplasms are thought to be related to Reserpine’s prolactin-elevating effect. Several other prolactin-elevating drugs have also been associated with an increased incidence of mammary neoplasia in rodents.
The extent to which these findings indicate a risk to humans is uncertain. Tissue culture experiments show that about one third of human breast tumors are prolactin-dependent in vitro, a factor of considerable importance if the use of the drug is contemplated in a patient with previously detected breast cancer. The possibility of an increased risk of breast cancer in Reserpine users has been studied extensively; however, no firm conclusion has emerged. Although a few epidemiologic studies have suggested a slightly increased risk (less than twofold in all studies except one) in women who have used Reserpine, other studies of generally similar design have not confirmed this. Epidemiologic studies conducted using other drugs (neuroleptic agents) that, like Reserpine, increase prolactin levels and therefore would be considered rodent mammary carcinogens have not shown an association between chronic administration of the drug and human mammary tumorigenesis. While long-term clinical observation has not suggested such as association, the available evidence is considered too limited to be conclusive at this time. An association of Reserpine intake with pheochromocytoma or tumors of the seminal vesicles has not been explored.
Pregnancy Category C
Reserpine administered parenterally has been shown to be teratogenic in rats at doses up to 2 mg/kg and to have an embryocidal effect in guinea pigs given dosages of 0.5 mg daily.
There are no adequate and well-controlled studies of Reserpine in pregnant women. Reserpine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.Nonteratogenic Effects
Reserpine crosses the placental barrier, and increased respiratory tract secretions, nasal congestion, cyanosis, and anorexia may occur in neonates of Reserpine-treated mothers.
Reserpine is excreted in maternal breast milk, and increased respiratory tract secretions, nasal congestion, cyanosis, and anorexia may occur in breast-fed infants. Because of the potential for adverse reactions in nursing infants and the potential for tumorigenicity shown for Reserpine in animal studies, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
Safety and effectiveness in children have not been established by means of controlled clinical trials, although there is experience with the use of Reserpine in children (see DOSAGE AND ADMINISTRATION.) Because of adverse effects such as emotional depression and lability, sedation, and stuffy nose, Reserpine is not usually recommended as a step-2 drug in the treatment of hypertension in children.
The following adverse reactions have been observed with rauwolfia preparations, but there has not been enough systematic collection of data to support an estimate of their frequency. Consequently the reactions are categorized by organ system and are listed in decreasing order of severity and not frequency.
Vomiting, diarrhea, nausea, anorexia, dryness of mouth, hypersecretion.
Arrhythmias (particularly when used concurrently with digitalis or quinidine), syncope, angina-like symptoms, bradycardia, edema.
Dyspnea, epistaxis, nasal congestion.
Rare parkinsonian syndrome and other extrapyramidal tract symptoms; dizziness; headache; paradoxical anxiety; depression; nervousness; nightmares; dull sensorium; drowsiness.
Pseudolactation, impotence, dysuria, gynecomastia, decreased libido, breast engorgement.
Deafness, optic atrophy, glaucoma, uveitis, conjunctival injection.
Purpura, rash, pruritus.
No deaths due to acute poisoning with Reserpine have been reported.
Highest known doses survived: children, 1000 mg (age and sex not specified); young children, 200 mg (20-month-old boy).
Oral LD50's in animals (mg/kg): rat, 2993; mouse, 47 and 500.
Signs and Symptoms
The clinical picture of acute poisoning is characterized chiefly by signs and symptoms due to the reflex parasympathomimetic effect of Reserpine.
Impairment of consciousness may occur and may range from drowsiness to coma, depending upon the severity of overdosage. Flushing of the skin, conjunctival injection, and pupillary constriction are to be expected. Hypotension, hypothermia, central respiratory depression, and bradycardia may develop in cases of severe overdosage. Increased salivary and gastric secretion and diarrhea may also occur.
There is no specific antidote.
Stomach contents should be evacuated, taking adequate precautions against aspiration and for protection of the airway. Activated charcoal slurry should be instilled.
The effects of Reserpine overdosage should be treated symptomatically. If hypotension is severe enough to require treatment with a vasopressor, one having a direct action upon vascular smooth muscle (e.g., phenylephrine, levarterenol, metaraminol) should be used. Since Reserpine is long-acting, the patient should be observed carefully for at least 72 hours, and treatment administered as required.
Reserpine Dosage and Administration
In the average patient not receiving other antihypertensive agents, the usual initial dosage is 0.5 mg daily for 1 or 2 weeks., For maintenance, reduce to 0.1-0.25 mg daily. Higher dosages should be used cautiously, because occurrence of serious mental depression and other side effects may increase considerably.
The usual initial dosage is 0.5 mg daily, but may range from 0.1 mg to 1.0 mg. Adjust dosage upward or downward according to the patient's response.
Reserpine is not recommended for use in children (see PRECAUTIONS: Pediatric Use). If it is to be used in treating a child, the usual recommended starting dose is 20 µg/kg daily. The maximum recommended dose is 0.25 mg (total) daily.
How is Reserpine Supplied
Reserpine Tablets, USP for oral administration are available as:
0.1 mg: round, white, scored tablets, debossed SZ 71 on one side and plain on the reverse side and supplied as:
NDC 0185-0032-01 bottles of 100
NDC 0185-0032-10 bottles of 1000
0.25 mg: round, white, scored tablets, debossed SZ 77 on one side and plain on the reverse side and supplied as:
NDC 0185-0134-01 bottles of 100
NDC 0185-0134-10 bottles of 1000
Store at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature]. Protect from moisture.
Preserve in tight, light-resistant containers.
Princeton, NJ 08540
0.1 mg Label
0.25 mg Label
|Labeler - Eon Labs, Inc. (012656273)|