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TOXICITY TO VARIOUS AGENTS ( 50 FDA reports)
COMPLETED SUICIDE ( 45 FDA reports)
RESPIRATORY ARREST ( 38 FDA reports)
CARDIAC ARREST ( 37 FDA reports)
INTENTIONAL DRUG MISUSE ( 33 FDA reports)
NAUSEA ( 16 FDA reports)
DIARRHOEA ( 12 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
DEHYDRATION ( 10 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
VOMITING ( 8 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
PANCREATITIS RELAPSING ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FALL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
PAIN ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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