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

DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
DRUG ABUSER ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
POLYSUBSTANCE ABUSE ( 7 FDA reports)
DEPRESSION ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
ALCOHOL USE ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
PAIN ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FALL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
POISONING ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRESS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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