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

NAUSEA ( 12 FDA reports)
BACK PAIN ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
FALL ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
PAIN ( 7 FDA reports)
VOMITING ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COUGH ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
INJURY ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
POLYP ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
STRESS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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