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

TACHYCARDIA ( 12 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE ( 9 FDA reports)
HYPOTENSION ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
CONVULSION ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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