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

DRUG INTERACTION ( 31 FDA reports)
BLOOD CREATININE INCREASED ( 24 FDA reports)
DYSPNOEA ( 23 FDA reports)
PYREXIA ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 17 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
RENAL FAILURE ( 14 FDA reports)
COLITIS ( 12 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 11 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
COMA ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
RHABDOMYOLYSIS ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DEATH ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
SHOCK HYPOGLYCAEMIC ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
KETOSIS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
LOCALISED INFECTION ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
FALL ( 4 FDA reports)
GESTATIONAL DIABETES ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOPRAXIA ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES GESTATIONIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARYNGITIS BACTERIAL ( 1 FDA reports)
LARYNGITIS FUNGAL ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCAN THYROID GLAND ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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