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

INFLAMMATORY BOWEL DISEASE ( 54 FDA reports)
PYREXIA ( 44 FDA reports)
ANXIETY ( 40 FDA reports)
ARTHRALGIA ( 34 FDA reports)
ABDOMINAL PAIN ( 31 FDA reports)
CROHN'S DISEASE ( 30 FDA reports)
AUTOIMMUNE THYROIDITIS ( 28 FDA reports)
ILEITIS ( 28 FDA reports)
COLITIS ( 27 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 27 FDA reports)
RECTAL HAEMORRHAGE ( 26 FDA reports)
CYST ( 25 FDA reports)
DRUG INTERACTION ( 25 FDA reports)
COLITIS ULCERATIVE ( 24 FDA reports)
DEPRESSION ( 24 FDA reports)
DYSPNOEA ( 23 FDA reports)
STRESS URINARY INCONTINENCE ( 23 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
UTERINE PROLAPSE ( 23 FDA reports)
EYE INFLAMMATION ( 22 FDA reports)
OEDEMA ( 22 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 21 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 21 FDA reports)
SUICIDE ATTEMPT ( 21 FDA reports)
VOMITING ( 21 FDA reports)
DIZZINESS ( 20 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 18 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
ASCITES ( 17 FDA reports)
HEPATIC ENZYME INCREASED ( 16 FDA reports)
ANAEMIA ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
LIP DRY ( 14 FDA reports)
DRY SKIN ( 13 FDA reports)
EMOTIONAL DISTRESS ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
INJURY ( 13 FDA reports)
IRRITABLE BOWEL SYNDROME ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
POLYP ( 13 FDA reports)
PROCTITIS ( 13 FDA reports)
CHOLANGITIS ( 12 FDA reports)
HYPERBILIRUBINAEMIA ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
PAIN ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
PROCTOCOLITIS ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
DEHYDRATION ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
MUCOSAL INFLAMMATION ( 8 FDA reports)
PERINEAL LACERATION ( 8 FDA reports)
POSTPARTUM HAEMORRHAGE ( 8 FDA reports)
RASH ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
COUGH ( 7 FDA reports)
FOOT DEFORMITY ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ACNE ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GESTATIONAL HYPERTENSION ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GALLBLADDER OEDEMA ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MUCOSAL HAEMORRHAGE ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERIOSTITIS ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FALL ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPLANT EVALUATION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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