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

AGGRESSION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
TIC ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EYE PROSTHESIS USER ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STICKLER'S SYNDROME ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)