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

PNEUMONIA ASPIRATION ( 9 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
ILEUS ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANGER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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