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

DRUG INTERACTION ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
AGITATION ( 3 FDA reports)
BRUGADA SYNDROME ( 3 FDA reports)
COMA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOANING ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SPINDLE CELL SARCOMA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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