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

MULTIPLE DRUG OVERDOSE ( 21 FDA reports)
AGITATION ( 10 FDA reports)
COMA ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
POLYSUBSTANCE ABUSE ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CYST ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND ( 1 FDA reports)
YAWNING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use