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

DYSPNOEA ( 37 FDA reports)
HYPOTENSION ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
DIARRHOEA ( 27 FDA reports)
RENAL FAILURE ( 25 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
DIZZINESS ( 20 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
HYPERTENSION ( 19 FDA reports)
VOMITING ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
DRUG INTERACTION ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
DEATH ( 15 FDA reports)
DYSARTHRIA ( 15 FDA reports)
FATIGUE ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
PHARYNGITIS ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 12 FDA reports)
OTITIS MEDIA ACUTE ( 12 FDA reports)
PATHOLOGICAL GAMBLING ( 12 FDA reports)
PSYCHIATRIC SYMPTOM ( 12 FDA reports)
RHINITIS ALLERGIC ( 12 FDA reports)
TRACHEITIS ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
FALL ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
COUGH ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 7 FDA reports)
AGITATION ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PAIN ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
COMA ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INFECTION ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
RASH ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ANURIA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RALES ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD IRON 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 DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BOWENOID PAPULOSIS ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
REBOUND HYPERTENSION ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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