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.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Modopar Safety Reports submitted to FDA

Total Modopar reports: 5.
Modopar FDA safety alerts: No.
Reported deaths: 4    Reported hospitalizations: 5.
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Reported Modopar Side Effects: hypoglycaemic coma, hypertonia, hallucination, visual, haematemesis, confusional state, c-reactive protein increased, blood urea increased, blood glucose increased, asthenia, pyrexia, pulmonary hypertension.
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Modopar Side Effects Report #5243773-0
Consumer or non-health professional from FRANCE reported MODOPAR problem on Feb 19, 2007. Female patient, 96 years of age, weighting 121.3 lb, was treated with MODOPAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood glucose increased, blood urea increased, c-reactive protein increased, confusional state, haematemesis, hallucination, visual, hypertonia, hypoglycaemic coma. MODOPAR dosage: unknown. During the same period patient was treated with TRIVASTAL, DAFLON, METEOXANE, MOVICOL, SERESTA, KARDEGIC, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE MAGNESIUM. Patient was hospitalized. Patient died on 11/14/2006.

Modopar Side Effects Report #5261801-3
MODOPAR problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2007. Female patient, 96 years of age, weighting 121.3 lb, was treated with MODOPAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood glucose increased, blood urea increased, c-reactive protein increased, confusional state, haematemesis, hallucination, visual, hypertonia, hypoglycaemic coma. MODOPAR dosage: unknown. During the same period patient was treated with TRIVASTAL, DAFLON, METEOXANE, MOVICOL, SERESTA, KARDEGIC, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE MAGNESIUM. Patient was hospitalized. Patient died on 11/14/2006.

Modopar Side Effects Report #5264647-5
Consumer or non-health professional from FRANCE reported MODOPAR problem on Mar 05, 2007. Female patient, 96 years of age, weighting 121.3 lb, was treated with MODOPAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood glucose increased, blood urea increased, c-reactive protein increased, confusional state, haematemesis, hallucination, visual, hypertonia, hypoglycaemic coma. MODOPAR dosage: unknown. During the same period patient was treated with TRIVASTAL, DAFLON, METEOXANE, MOVICOL, SERESTA, KARDEGIC, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE MAGNESIUM. Patient was hospitalized. Patient died on 11/14/2006.

Modopar Side Effects Report #5264759-6
MODOPAR problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2007. Female patient, 96 years of age, weighting 121.3 lb, was treated with MODOPAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood glucose increased, blood urea increased, c-reactive protein increased, confusional state, haematemesis, hallucination, visual, hypertonia, hypoglycaemic coma. MODOPAR dosage: unknown. During the same period patient was treated with TRIVASTAL, DAFLON, METEOXANE, MOVICOL, SERESTA, KARDEGIC, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE MAGNESIUM. Patient was hospitalized. Patient died on 11/14/2006.

Modopar Side Effects Report #5078467-8
Consumer or non-health professional from FRANCE reported MODOPAR problem on Aug 07, 2006. Female patient, 76 years of age, was diagnosed with parkinson's disease and was treated with MODOPAR. After drug was administered, patient experienced the following problems/side effects: brain natriuretic peptide increased, cardiac murmur, dyspnoea, mitral valve incompetence, productive cough, pulmonary hypertension, pyrexia. MODOPAR dosage: unknown. During the same period patient was treated with REQUIP, COMTAN. Patient was hospitalized. Patient recovered.

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