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

PLATELET COUNT DECREASED ( 44 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 37 FDA reports)
PNEUMONIA ( 36 FDA reports)
PYREXIA ( 35 FDA reports)
NAUSEA ( 34 FDA reports)
HAEMOGLOBIN DECREASED ( 31 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 29 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 29 FDA reports)
BLOOD CREATININE INCREASED ( 27 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 27 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 26 FDA reports)
MALAISE ( 26 FDA reports)
DIZZINESS ( 25 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
INTERSTITIAL LUNG DISEASE ( 23 FDA reports)
DIARRHOEA ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
ANAEMIA ( 21 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 20 FDA reports)
VOMITING ( 20 FDA reports)
BLOOD UREA INCREASED ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 18 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 18 FDA reports)
LIVER DISORDER ( 17 FDA reports)
RASH ( 16 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
GRANULOCYTOPENIA ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
SEPTIC SHOCK ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
DRUG LEVEL INCREASED ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
CHEST X-RAY ABNORMAL ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
ESCHERICHIA INFECTION ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
ABASIA ( 7 FDA reports)
ANURIA ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
LARGE INTESTINE PERFORATION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EYELID FUNCTION DISORDER ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
NEOPLASM PROSTATE ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CUTANEOUS TUBERCULOSIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PYOTHORAX ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SURGERY ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PROSTATIC ABSCESS ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
SCAR ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOSCOPY SMALL INTESTINE ( 2 FDA reports)
EXTRADURAL ABSCESS ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SCLERODERMA RENAL CRISIS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSYCHOLOGICAL FACTOR AFFECTING MEDICAL CONDITION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

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