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

HEADACHE ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
FALL ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SWELLING ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STARING ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)

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