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| __NOTOC__
| | #REDIRECT [[Reserpine#Nonclinical Toxicology]] |
| {{Reserpine}}
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| {{CMG}}; {{AE}} {{AK}}
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| ==Nonclinical Toxicology==
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| ===Carcinogenesis, Mutagenesis, Impairment of Fertility===
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| ====Animal Tumorigenicity====
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| 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.
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| 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.
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| ====Pregnancy Category C====
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| 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.
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| 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.
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| ===Nonteratogenic Effects===
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| Reserpine crosses the placental barrier, and increased respiratory tract secretions, nasal congestion, cyanosis, and anorexia may occur in neonates of reserpine-treated mothers.
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| ===Nursing Mothers===
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| 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.
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| ===Pediatric Use===
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| 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 [[Reserpine dosage and administration|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<ref name="dailymed.nlm.nih.gov">{{Cite web | last = | first = | title = RESERPINE TABLET [EON LABS, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a4d74d7-2e63-4789-b50e-af17ced92462 | publisher = | date = | accessdate = 7 March 2014 }}</ref>
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| ==References==
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| {{Reflist|2}}
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| [[Category:Cardiovascular Drugs]]
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| [[Category:Drugs]]
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