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

OEDEMA PERIPHERAL ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
INFECTION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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