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

DRUG INTERACTION ( 47 FDA reports)
RENAL FAILURE ACUTE ( 47 FDA reports)
THROMBOCYTOPENIA ( 44 FDA reports)
FALL ( 35 FDA reports)
DIARRHOEA ( 34 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 34 FDA reports)
HAEMATOMA ( 29 FDA reports)
ANAEMIA ( 28 FDA reports)
SOMNOLENCE ( 23 FDA reports)
DYSPNOEA ( 22 FDA reports)
HYPERKALAEMIA ( 22 FDA reports)
MALAISE ( 22 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
PYREXIA ( 19 FDA reports)
PRURITUS ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
DEHYDRATION ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
PAIN ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
VOMITING ( 15 FDA reports)
BRADYCARDIA ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
OEDEMA ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
LEUKOPENIA ( 13 FDA reports)
MELAENA ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
ESCHERICHIA SEPSIS ( 11 FDA reports)
RASH ERYTHEMATOUS ( 11 FDA reports)
CONVULSION ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
RALES ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
BACK PAIN ( 9 FDA reports)
BRONCHIAL OBSTRUCTION ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
SKIN EXFOLIATION ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
DEATH ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DERMATITIS EXFOLIATIVE ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
IMPETIGO ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
LEUKOCYTOSIS ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
SHOCK ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TREMOR ( 6 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
BREAST OEDEMA ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PNEUMONIA ESCHERICHIA ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
THROMBOEMBOLECTOMY ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CULTURE WOUND POSITIVE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GLOBULINS DECREASED ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATOJUGULAR REFLUX ( 4 FDA reports)
HYPOCOMPLEMENTAEMIA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TUBERCULOSIS BLADDER ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
PENIS CARCINOMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
SCROTAL CANCER ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARASITIC GASTROENTERITIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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