Medrol and international normalised ratio increased Patient Reports February 10, 2012

Medrol Side Effects Report #4686294-6
Medrol side effect was reported by a Physician from on May 24, 2005. Female patient, 83 years of age, weighting 116.8 lb, was diagnosed with lung infection, ill-defined disorder and was treated with Medrol. After drug was administered, patient experienced the following side effects: abdominal wall disorder, anaemia, blood creatine phosphokinase increased, fall , haematoma, infection , international normalised ratio increased, platelet count decreased. Medrol dosage: 16 MG (16 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PREVISCAN, FULID, OMEPRAZOLE, CITALOPRAM HYDROBROMIDE, ALPRAZOLAM, TANAKAN, MOVICOL. Patient was hospitalized. Patient recovered.

Medrol Side Effects Report #4875060-4
Medrol side effect was reported by a Pharmacist from UNITED STATES on Dec 20, 2005. Male patient, 62 years of age, weighting 160.9 lb, was diagnosed with ill-defined disorder, metastasis, lung neoplasm malignant and was treated with Medrol. After drug was administered, patient experienced the following side effects: abdominal pain upper, amyotrophy, body temperature decreased, deep vein thrombosis , duodenal ulcer, hiatus hernia, international normalised ratio increased, musculoskeletal chest pain, neutropenia. Medrol dosage: unknown. During the same period patient was treated with CISPLATIN, TEMODAL, GEMZAR, ASPIRIN, TAXOL. Patient was hospitalized. Patient recovered.

Medrol Side Effects Report #5192409-6
Medrol side effect was reported by a Health Professional from FRANCE on Dec 18, 2006. Female patient, 71 years of age, was diagnosed with bronchitis  and was treated with Medrol. After drug was administered, patient experienced the following side effects: back pain , international normalised ratio increased, muscle haemorrhage. Medrol dosage: unknown. During the same period patient was treated with FLUINDIONE, TELITHROMYCIN, AMBROXOL HYDROCHLORIDE, CODEINE. Patient was hospitalized. Patient recovered.

Medrol Side Effects Report #5074718-4
Medrol side effect was reported by a Physician from FRANCE on July 25, 2006. Female patient, 90 years of age, was treated with Medrol. After drug was administered, patient experienced the following side effects: erosive duodenitis, gastrointestinal haemorrhage, hypokalaemia, international normalised ratio increased, lower gastrointestinal haemorrhage, upper gastrointestinal haemorrhage. Medrol dosage: 4 MG (4 MG, 1 D), ORAL. During the same period patient was treated with SINTROM. Patient was hospitalized. Patient recovered.