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

PLATELET COUNT DECREASED ( 25 FDA reports)
INTERSTITIAL LUNG DISEASE ( 19 FDA reports)
DIARRHOEA ( 15 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
PYREXIA ( 12 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
NEUTROPHIL COUNT DECREASED ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
LUNG ADENOCARCINOMA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RASH ( 7 FDA reports)
ASCITES ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
MELAENA ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD CHLORIDE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
COMA ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIHEPATIC ABSCESS ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CERVICAL VERTEBRA INJURY ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARGE CELL LUNG CANCER METASTATIC ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OPTIC DISC VASCULAR DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)

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