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

DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 4 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
SPINA BIFIDA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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