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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes, said the Institute of Medicine report, released yesterday.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
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Zegerid Safety Reports submitted to FDA
Total
Zegerid reports: 4.
Zegerid FDA safety alerts:
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Reported Zegerid Side Effects: syncope, oedema peripheral, hyperhidrosis, dyspnoea, pain in extremity, dyspepsia, condition aggravated, cholelithiasis, burning sensation, arthralgia, blood pressure increased.
Zegerid Usage.
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Zegerid Side Effects Report #5208782-6
Consumer or non-health professional from UNITED STATES reported ZEGERID problem on Jan 11, 2007. Female patient was treated with ZEGERID. After drug was administered, patient experienced the following problems/side effects:
chest pain, dyspnoea, hyperhidrosis, nausea, oedema peripheral, syncope. ZEGERID dosage: 20 MG ORAL POWDER. Patient recovered.
Zegerid Side Effects Report #5268632-9
ZEGERID problem was reported by a Pharmacist from UNITED STATES on Mar 15, 2007. Male patient, weighting 225.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with ZEGERID. After drug was administered, patient experienced the following problems/side effects:
anxiety, blood pressure increased. ZEGERID dosage: 40MG DAILY PO. Patient recovered.
Zegerid Side Effects Report #5272597-3
Health Professional from UNITED STATES reported ZEGERID problem on Mar 20, 2007. Female patient, 50 years of age, weighting 190.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with ZEGERID. After drug was administered, patient experienced the following problems/side effects:
arthralgia, burning sensation, cholelithiasis, condition aggravated, dyspepsia, pain in extremity. ZEGERID dosage: 40 MG 1 CAPSULE A DAY PO. Patient recovered.
Zegerid Side Effects Report #5171377-7
ZEGERID problem was reported by a Health Professional from UNITED STATES on Dec 08, 2006. Female patient, 68 years of age, weighting 160.0 lb, was diagnosed with dyspepsia and was treated with ZEGERID. After drug was administered, patient experienced the following problems/side effects:
dyspnoea, hyperhidrosis, oedema peripheral, syncope. ZEGERID dosage: unknown. Patient recovered.
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