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

DRUG INEFFECTIVE ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SMOKER ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
RASH ( 3 FDA reports)
APHASIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
MANIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
ABASIA ( 2 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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