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

DRUG TOXICITY ( 24 FDA reports)
OVERDOSE ( 22 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 10 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
DEATH ( 7 FDA reports)
INFECTION ( 6 FDA reports)
FALL ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
AGITATION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
RASH ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CLINODACTYLY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
CHOANAL ATRESIA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)

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