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

BLOOD GLUCOSE INCREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
DIZZINESS ( 7 FDA reports)
FATIGUE ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STRESS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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