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

FEELING ABNORMAL ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
AURA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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