Medrol and condition aggravated Patient Reports February 10, 2012
Medrol Side Effects Report #4868623-3
Medrol side effect was reported by a Physician from FRANCE on Dec 12, 2005. Male patient, 64 years of age, was diagnosed with nervous system neoplasm and was treated with Medrol. After drug was administered, patient experienced the following side effects: condition aggravated, confusional state, disorientation. Medrol dosage: 64 MG, ORAL. During the same period patient was treated with OMEPRAZOLE, NEURONTIN, NITRIDERM TTS, BISOPROLOL FUMARATE, LEXOMIL. Patient was hospitalized. Patient recovered.
Medrol Side Effects Report #4909946-9
Medrol side effect was reported by a Physician from FRANCE on Jan 27, 2006. Male patient, 58 years of age, weighting 138.9 lb, was diagnosed with ill-defined disorder and was treated with Medrol. After drug was administered, patient experienced the following side effects: condition aggravated, confusional state, diabetes mellitus, disorientation, hyponatraemia, pulmonary congestion, respiratory failure. Medrol dosage: 1 DF (100 MG), ORAL. During the same period patient was treated with VALPROIC ACID. Patient was hospitalized. Patient died on 10/18/2005.
Medrol Side Effects Report #4600663-1
Medrol side effect was reported by a Physician from on Feb 17, 2005. Female patient, 53 years of age, was diagnosed with ill-defined disorder and was treated with Medrol. After drug was administered, patient experienced the following side effects: acute respiratory distress syndrome, condition aggravated, diabetes mellitus, iatrogenic injury, infection in an immunocompromised host, interstitial lung disease, pneumocystis jiroveci infection, respiratory failure. Medrol dosage: 64 MG (32 MG, INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with ACETYLCYSTEINE, LAMOTRIGINE, CLOBAZAM, OMEPRAZOLE. Patient died on 07/09/2003.
Medrol Side Effects Report #4603083-9
Medrol side effect was reported by a Physician from on Feb 22, 2005. Female patient, 53 years of age, was diagnosed with ill-defined disorder and was treated with Medrol. After drug was administered, patient experienced the following side effects: acute respiratory distress syndrome, condition aggravated, diabetes mellitus, interstitial lung disease, pneumocystis jiroveci pneumonia, respiratory failure. Medrol dosage: 64 MG (32 MG, INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with ACETYLCYSTEINE, LAMOTRIGINE, CLOBAZAM, OMEPRAZOLE. Patient died on 07/09/2003.
Medrol Side Effects Report #4727726-4
Medrol side effect was reported by a Physician from INDIA on July 11, 2005. Female patient was diagnosed with asthma
and was treated with Medrol. After drug was administered, patient experienced the following side effects: asthma
, condition aggravated. Medrol dosage: 4 MG, ORAL. Patient was hospitalized. Patient recovered.Medrol Side Effects Report #4728130-5
Medrol side effect was reported by a Physician from INDIA on July 11, 2005. Female patient was diagnosed with asthma
and was treated with Medrol. After drug was administered, patient experienced the following side effects: asthma
, condition aggravated. Medrol dosage: (4 MG), ORAL. Patient was hospitalized. Patient recovered.Medrol Side Effects Report #4728131-7
Medrol side effect was reported by a Physician from INDIA on July 11, 2005. Female patient was diagnosed with asthma
and was treated with Medrol. After drug was administered, patient experienced the following side effects: asthma
, condition aggravated. Medrol dosage: unknown. Patient was hospitalized. Patient recovered.
Medrol and condition aggravated 