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OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional.

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Animal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

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Risk factors for gastrointestinal obstruction identified from post-marketing reports of Procardia XL (GITS tablet formulation) include alteration in gastrointestinal anatomy (severe gastrointestinal narrowing, colon cancer, small bowel obstruction, bowel resection, gastric bypass, vertical banded gastroplasty, and colostomy), hypomotility disorders (constipation, gastroesophageal reflux disease, ileus, obesity, hypothyroidism, and diabetes) and concomitant medications (H2-histamine blockers, nonsteroidal antiinflammatory drugs, laxatives, anticholinergic agents, and levothyroxine).

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The problem of small size, which plagued earlier investigations, was resolved with the publication during the 1990s of a number of studies of sufficient magnitude and statistical power (300 to 1000 patients followed up over 1 to 3 years) to answer with confidence the question of the importance of silent ischemia on ambulatory monitoring.

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Las companías fármacas que producen las versiones genéricas, solamente deben comprar una fórmula química y gastar dinero en la producción.

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The increase in ocular blood flow without increase in intraocular pressure applies to healthy controls as well, although the visual ramifications of this are not clear (ie.

This review will address the pharmacology, pharmacokinetics and the available clinical trial data on long-acting nifedipine and summarize its role in the management of hypertension.

Las drogas genéricas son los mismos productos, como los de Brand, pero ellos están producidos y distribuídos sin defensa del patente.

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The most common side effect reported with PROCARDIA XL was edema which was dose related and ranged in frequency from approximately 10% to about 30% at the highest dose studied (180 mg).

Cases of tablet adherence to the gastrointestinal wall with ulceration have been reported, some requiring hospitalization and intervention.

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