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

SUDDEN DEATH ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DELUSION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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