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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.
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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Review Cephadol Safety Reports submitted to FDA

Total Cephadol reports: 4.
Cephadol FDA safety alerts: No.
Reported deaths: 4    Reported hospitalizations: 4.
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FDA Reported Cephadol Side Effects: dehydration, c-reactive protein increased, blood urea increased, blood pressure decreased, blood creatinine increased, blood creatine phosphokinase increased, blood bilirubin increased, aspartate aminotransferase increased, alanine aminotransferase increased.
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Cephadol Side Effects Report #5387285-2
Consumer or non-health professional from JAPAN reported CEPHADOL problem on July 11, 2007. Female patient, 66 years of age, weighting 119.0 lb, was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and was treated with CEPHADOL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. CEPHADOL dosage: unknown. During the same period patient was treated with URALYT, ALLOPURINOL, NOVAMIN, TICLOPIDINE, MERISLON, GLEEVEC. Patient was hospitalized. Patient died.

Cephadol Side Effects Report #5393335-X
CEPHADOL problem was reported by a Consumer or non-health professional from JAPAN on July 19, 2007. Female patient, 66 years of age, weighting 119.0 lb, was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and was treated with CEPHADOL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. CEPHADOL dosage: unknown. During the same period patient was treated with URALYT, ALLOPURINOL, NOVAMIN, TICLOPIDINE, MERISLON, GLEEVEC. Patient was hospitalized. Patient died on 10/10/2006.

Cephadol Side Effects Report #5387285-2
Consumer or non-health professional from JAPAN reported CEPHADOL problem on July 11, 2007. Female patient, 66 years of age, weighting 119.0 lb, was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and was treated with CEPHADOL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. CEPHADOL dosage: unknown. During the same period patient was treated with URALYT, ALLOPURINOL, NOVAMIN, TICLOPIDINE, MERISLON, GLEEVEC. Patient was hospitalized. Patient died.

Cephadol Side Effects Report #5393335-X
CEPHADOL problem was reported by a Consumer or non-health professional from JAPAN on July 19, 2007. Female patient, 66 years of age, weighting 119.0 lb, was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and was treated with CEPHADOL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. CEPHADOL dosage: unknown. During the same period patient was treated with URALYT, ALLOPURINOL, NOVAMIN, TICLOPIDINE, MERISLON, GLEEVEC. Patient was hospitalized. Patient died on 10/10/2006.


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alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration, , was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and was diagnosed with dizziness, hyperuricaemia, nausea, chronic myeloid leukaemia and