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

PARANASAL CYST ( 4 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
JOINT DEPOSIT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
REDUCED BLADDER CAPACITY ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
KNEE OPERATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
PRETERNATURAL ANUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)

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