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

NAUSEA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
PAIN ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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