To determine which antitubercular drug inhibits the action of oral contraceptive pills (OCPs), we need to understand the interaction between these drugs and enzyme induction pathways in the liver.
Rifampicin, a commonly used antitubercular drug, is known to be a potent inducer of cytochrome P450 (CYP) enzymes, specifically CYP3A4. This enzyme induction increases the metabolism of various drugs, including the hormones found in oral contraceptives. As a result, the effectiveness of the OCPs is reduced, which may lead to contraceptive failure.
In contrast, Ethambutol, Isoniazid, and Pyrazinamide do not have significant enzyme-inducing effects and thus do not notably affect the efficacy of oral contraceptives.
Therefore, the drug that inhibits the action of OCPs by inducing their metabolism is Rifampicin.
The most common site of metastasis for breast cancer is:
Which of the following cranial nerves is responsible for the motor innervation of the muscles of mastication?
The primary source of energy for Earth’s climate system is:-
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Which enzyme is deficient in Gaucher’s disease?