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

CONDITION AGGRAVATED ( 29 FDA reports)
PYREXIA ( 29 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
MALAISE ( 20 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
RENAL FAILURE CHRONIC ( 19 FDA reports)
NAUSEA ( 17 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
FALL ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
ANOREXIA ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
HYPERCALCAEMIA ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
EMPHYSEMA ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HILAR LYMPHADENOPATHY ( 9 FDA reports)
PANCREATIC ATROPHY ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
TREMOR ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
RASH ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GRANULOMA ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFECTION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
OESOPHAGEAL STENOSIS ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
SCAR ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCALCIURIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TETANY ( 2 FDA reports)
THIRST ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIUM PHOSPHATE PRODUCT INCREASED ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CSF PROTEIN ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIARRHOEA NEONATAL ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOLLICULAR MUCINOSIS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFANTILE ASTHMA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRUANCY ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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