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

PNEUMONIA ( 4 FDA reports)
HEADACHE ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
RASH ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
FALL ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
CYST ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
CATARACT ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)

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