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

SOMNOLENCE ( 23 FDA reports)
TACHYCARDIA ( 21 FDA reports)
COMA ( 19 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
FATIGUE ( 17 FDA reports)
SUICIDE ATTEMPT ( 17 FDA reports)
WEIGHT INCREASED ( 17 FDA reports)
GAIT DISTURBANCE ( 16 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
RESTLESSNESS ( 12 FDA reports)
AGGRESSION ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
CHILLS ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
AGITATION ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
FEELING DRUNK ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INDIFFERENCE ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LOSS OF LIBIDO ( 8 FDA reports)
PERIPHERAL COLDNESS ( 8 FDA reports)
POOR PERIPHERAL CIRCULATION ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
ATRIAL FLUTTER ( 7 FDA reports)
BLOOD PROLACTIN INCREASED ( 7 FDA reports)
BREAST DISCOMFORT ( 7 FDA reports)
BREAST ENLARGEMENT ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
TREMOR ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
DISORIENTATION ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC ENZYME DECREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
LONG QT SYNDROME ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHASIA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SOPOR ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MASS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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