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

PYREXIA ( 22 FDA reports)
RENAL FAILURE ACUTE ( 22 FDA reports)
FALL ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
DYSPNOEA ( 18 FDA reports)
HYPONATRAEMIA ( 18 FDA reports)
DRUG INTERACTION ( 17 FDA reports)
RENAL FAILURE ( 16 FDA reports)
CONFUSIONAL STATE ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
VOMITING ( 13 FDA reports)
CORONARY ARTERY STENOSIS ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
BRADYCARDIA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
PANCYTOPENIA ( 11 FDA reports)
TOXIC SKIN ERUPTION ( 11 FDA reports)
CONVULSION ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
MALAISE ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PAIN ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
DEATH ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
COMA ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THIRST ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VITAMIN B1 DEFICIENCY ( 2 FDA reports)
VITAMIN B6 DEFICIENCY ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PRIMARY HYPOGONADISM ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE CLOT IN BLOOD PRESENT ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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