Please choose an event type to view the corresponding MedsFacts report:

ANAL FISTULA INFECTION ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
VIRAEMIA ( 2 FDA reports)
VESICOURETERIC REFLUX ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
EYE INFECTION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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