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

PYREXIA ( 147 FDA reports)
DYSPNOEA ( 95 FDA reports)
MYOCARDIAL INFARCTION ( 92 FDA reports)
ANAEMIA ( 84 FDA reports)
NEUTROPENIA ( 84 FDA reports)
ANGINA PECTORIS ( 82 FDA reports)
CHEST PAIN ( 79 FDA reports)
PNEUMONIA ( 79 FDA reports)
CORONARY ANGIOPLASTY ( 67 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 66 FDA reports)
CHEST DISCOMFORT ( 65 FDA reports)
MUSCULAR WEAKNESS ( 65 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 64 FDA reports)
THROMBOCYTOPENIA ( 58 FDA reports)
PAIN IN EXTREMITY ( 57 FDA reports)
CORONARY ARTERY RESTENOSIS ( 50 FDA reports)
HYPOAESTHESIA ( 49 FDA reports)
PALLOR ( 49 FDA reports)
COLD SWEAT ( 47 FDA reports)
CRANIOTOMY ( 47 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 47 FDA reports)
MOTOR DYSFUNCTION ( 47 FDA reports)
PAINFUL RESPIRATION ( 47 FDA reports)
PERIPHERAL COLDNESS ( 47 FDA reports)
SHUNT MALFUNCTION ( 47 FDA reports)
SUBDURAL HAEMATOMA ( 47 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 47 FDA reports)
PLATELET COUNT DECREASED ( 46 FDA reports)
CORONARY ARTERY STENOSIS ( 44 FDA reports)
CARDIAC FAILURE ( 38 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 37 FDA reports)
MOUTH ULCERATION ( 37 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 34 FDA reports)
BRONCHITIS ( 34 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 34 FDA reports)
LIVER DISORDER ( 34 FDA reports)
COUGH ( 33 FDA reports)
VASCULAR GRAFT ( 33 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 32 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 32 FDA reports)
GRAFT THROMBOSIS ( 32 FDA reports)
INSOMNIA ( 32 FDA reports)
LIMB OPERATION ( 32 FDA reports)
TOE AMPUTATION ( 32 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
CORONARY ARTERY DISEASE ( 30 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
PLEURAL EFFUSION ( 29 FDA reports)
STOMATITIS ( 28 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 27 FDA reports)
MELAENA ( 27 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
DRUG INEFFECTIVE ( 24 FDA reports)
EATING DISORDER ( 24 FDA reports)
FALL ( 24 FDA reports)
HEPATITIS VIRAL ( 24 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 24 FDA reports)
HYPERTENSION ( 24 FDA reports)
ORAL PAIN ( 24 FDA reports)
SEPSIS ( 24 FDA reports)
STENT PLACEMENT ( 23 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 22 FDA reports)
EPISTAXIS ( 22 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
BLOOD GLUCOSE INCREASED ( 21 FDA reports)
DIZZINESS ( 21 FDA reports)
FEBRILE NEUTROPENIA ( 21 FDA reports)
MALAISE ( 21 FDA reports)
MYOCARDIAL ISCHAEMIA ( 21 FDA reports)
PAIN ( 21 FDA reports)
SYNCOPE ( 21 FDA reports)
LIPASE INCREASED ( 20 FDA reports)
NAUSEA ( 20 FDA reports)
CORONARY ARTERY BYPASS ( 19 FDA reports)
ARTHRALGIA ( 18 FDA reports)
PRODUCTIVE COUGH ( 18 FDA reports)
RENAL FAILURE ( 18 FDA reports)
BACK PAIN ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
HYPERLIPIDAEMIA ( 17 FDA reports)
INTRACARDIAC THROMBUS ( 17 FDA reports)
NASOPHARYNGITIS ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
TACHYCARDIA ( 16 FDA reports)
VOMITING ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
ESCHERICHIA INFECTION ( 15 FDA reports)
KLEBSIELLA INFECTION ( 15 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
PULMONARY OEDEMA ( 15 FDA reports)
SEPTIC SHOCK ( 15 FDA reports)
HYPOTENSION ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
TROPONIN INCREASED ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
HAEMATOTOXICITY ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
PULMONARY CAVITATION ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
ARTERIOGRAM CORONARY ( 12 FDA reports)
CATHETERISATION CARDIAC ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
DYSPNOEA EXERTIONAL ( 12 FDA reports)
FLUID INTAKE REDUCED ( 12 FDA reports)
MONOCYTE COUNT DECREASED ( 12 FDA reports)
NECK PAIN ( 12 FDA reports)
RASH ( 12 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 10 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 10 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
INFECTION ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ARACHNOID CYST ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DEVICE RELATED INFECTION ( 9 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
EXERCISE TEST ABNORMAL ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
GINGIVITIS ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PERITONSILLAR ABSCESS ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
AORTIC CALCIFICATION ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DIABETIC VASCULAR DISORDER ( 8 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
MENINGITIS FUNGAL ( 8 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
INFECTIVE SPONDYLITIS ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
SWEAT GLAND DISORDER ( 7 FDA reports)
TONSILLITIS ( 7 FDA reports)
UTERINE DISORDER ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CORONARY REVASCULARISATION ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
ASCITES ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DYSCHEZIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FACIAL BONES FRACTURE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEMORAL ARTERY OCCLUSION ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
NASAL OEDEMA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
WOUND ( 5 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIP PAIN ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
ORAL DISCHARGE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CEREBELLAR HAEMATOMA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VENIPUNCTURE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY MUSCLE ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CORONARY ARTERY DILATATION ( 2 FDA reports)
CRANIECTOMY ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HYDROCELE OPERATION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAPUBIC CATHETER INSERTION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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