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

DRUG INTERACTION ( 40 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
DIARRHOEA ( 26 FDA reports)
LACTIC ACIDOSIS ( 24 FDA reports)
RENAL FAILURE ( 24 FDA reports)
NAUSEA ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
HYPOTENSION ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
VOMITING ( 21 FDA reports)
DIZZINESS ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
MYALGIA ( 15 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 12 FDA reports)
ARTHRALGIA ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
DEATH ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
FALL ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CHILLS ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
ALVEOLITIS ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HYPOGLYCAEMIC COMA ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ASCITES ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
COMA ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
RASH ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
APATHY ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
INCLUSION BODY MYOSITIS ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
POISONING ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITAMIN K DECREASED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BAROTITIS MEDIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WHITE BLOOD CELL AGGLUTINATION PRESENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BACTERIAL DNA TEST POSITIVE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METHYLMALONIC ACIDURIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use