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

PYREXIA ( 128 FDA reports)
PNEUMONIA ( 94 FDA reports)
ANAEMIA ( 89 FDA reports)
DECREASED APPETITE ( 85 FDA reports)
PLATELET COUNT DECREASED ( 83 FDA reports)
NAUSEA ( 82 FDA reports)
CONSTIPATION ( 81 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 78 FDA reports)
SEPSIS ( 78 FDA reports)
BLOOD CREATININE INCREASED ( 74 FDA reports)
MALAISE ( 72 FDA reports)
DIARRHOEA ( 68 FDA reports)
INTERSTITIAL LUNG DISEASE ( 68 FDA reports)
RENAL IMPAIRMENT ( 66 FDA reports)
HAEMOGLOBIN DECREASED ( 65 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 60 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 59 FDA reports)
DIZZINESS ( 59 FDA reports)
LIVER DISORDER ( 59 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 58 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 56 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 56 FDA reports)
BLOOD PRESSURE DECREASED ( 54 FDA reports)
VOMITING ( 54 FDA reports)
CARDIAC FAILURE ( 52 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 49 FDA reports)
BLOOD UREA INCREASED ( 48 FDA reports)
ANOREXIA ( 47 FDA reports)
DYSARTHRIA ( 45 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 44 FDA reports)
HALLUCINATION ( 43 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 42 FDA reports)
RASH ( 42 FDA reports)
BACK PAIN ( 41 FDA reports)
NEUTROPHIL COUNT DECREASED ( 41 FDA reports)
DEHYDRATION ( 40 FDA reports)
GAIT DISTURBANCE ( 40 FDA reports)
INSOMNIA ( 40 FDA reports)
PANCYTOPENIA ( 40 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 39 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 37 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 36 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 35 FDA reports)
RENAL FAILURE ACUTE ( 35 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 34 FDA reports)
HYPOAESTHESIA ( 34 FDA reports)
PLEURAL EFFUSION ( 34 FDA reports)
CONDITION AGGRAVATED ( 33 FDA reports)
MUSCULAR WEAKNESS ( 33 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
LOSS OF CONSCIOUSNESS ( 32 FDA reports)
PULMONARY OEDEMA ( 31 FDA reports)
DYSPNOEA ( 30 FDA reports)
OEDEMA ( 30 FDA reports)
THROMBOCYTOPENIA ( 30 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 30 FDA reports)
ABDOMINAL PAIN ( 29 FDA reports)
HEADACHE ( 29 FDA reports)
OEDEMA PERIPHERAL ( 29 FDA reports)
RHABDOMYOLYSIS ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 28 FDA reports)
ILEUS ( 28 FDA reports)
BLOOD GLUCOSE INCREASED ( 27 FDA reports)
MELAENA ( 27 FDA reports)
MULTI-ORGAN FAILURE ( 26 FDA reports)
NASOPHARYNGITIS ( 26 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HYPERTENSION ( 25 FDA reports)
PNEUMOTHORAX ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
STOMATITIS ( 25 FDA reports)
CEREBRAL INFARCTION ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
ENCEPHALOPATHY ( 24 FDA reports)
FALL ( 24 FDA reports)
OVERDOSE ( 24 FDA reports)
COUGH ( 23 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 23 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
TREMOR ( 23 FDA reports)
ABDOMINAL DISTENSION ( 22 FDA reports)
DELUSION ( 22 FDA reports)
DRUG INTERACTION ( 22 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 22 FDA reports)
PNEUMONIA ASPIRATION ( 22 FDA reports)
PRURITUS ( 22 FDA reports)
CLOSTRIDIUM COLITIS ( 21 FDA reports)
HYPOKALAEMIA ( 21 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 21 FDA reports)
RHINORRHOEA ( 21 FDA reports)
BLEEDING TIME PROLONGED ( 20 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 20 FDA reports)
HYPOGLYCAEMIA ( 20 FDA reports)
HYPOPROTEINAEMIA ( 20 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 20 FDA reports)
OPPORTUNISTIC INFECTION ( 20 FDA reports)
PSEUDOMONAS INFECTION ( 20 FDA reports)
RENAL DISORDER ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
ASTHENIA ( 19 FDA reports)
DEATH ( 19 FDA reports)
ABDOMINAL PAIN UPPER ( 18 FDA reports)
ANGINA PECTORIS ( 18 FDA reports)
DYSKINESIA ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
BLOOD SODIUM DECREASED ( 17 FDA reports)
BREAST CANCER ( 17 FDA reports)
CHEST DISCOMFORT ( 17 FDA reports)
CHOLANGITIS ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
DELIRIUM ( 17 FDA reports)
DRUG ERUPTION ( 17 FDA reports)
GASTRIC CANCER ( 17 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
INTESTINAL OBSTRUCTION ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
RESTLESSNESS ( 17 FDA reports)
ABNORMAL BEHAVIOUR ( 16 FDA reports)
ARTHRALGIA ( 16 FDA reports)
BRADYCARDIA ( 16 FDA reports)
NEOPLASM PROGRESSION ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
RENAL FAILURE CHRONIC ( 16 FDA reports)
SPEECH DISORDER ( 16 FDA reports)
ANXIETY ( 15 FDA reports)
CHILLS ( 15 FDA reports)
COMA ( 15 FDA reports)
DISORIENTATION ( 15 FDA reports)
DYSPHONIA ( 15 FDA reports)
INFECTION ( 15 FDA reports)
NEUTROPENIA ( 15 FDA reports)
PERITONITIS ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
OXYGEN SATURATION DECREASED ( 14 FDA reports)
SHOCK ( 14 FDA reports)
ASCITES ( 13 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
LARGE INTESTINE PERFORATION ( 13 FDA reports)
MOVEMENT DISORDER ( 13 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 13 FDA reports)
PROSTATE CANCER ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
SUDDEN DEATH ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
AGRANULOCYTOSIS ( 12 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
PURPURA ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
ALOPECIA ( 11 FDA reports)
AORTIC CALCIFICATION ( 11 FDA reports)
CANCER PAIN ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CATHETERISATION CARDIAC ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 11 FDA reports)
HAEMATURIA ( 11 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
INFLAMMATION ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
OROPHARYNGEAL PAIN ( 11 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 11 FDA reports)
VISUAL FIELD DEFECT ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 10 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
DIVERTICULITIS ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
GENERALISED OEDEMA ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HALLUCINATION, VISUAL ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
PAIN ( 10 FDA reports)
PARONYCHIA ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
PROTEINURIA ( 10 FDA reports)
REFLUX OESOPHAGITIS ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
WOUND ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
ESCHERICHIA INFECTION ( 9 FDA reports)
HAEMATEMESIS ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
INTESTINAL DILATATION ( 9 FDA reports)
LEUKOPENIA ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
PNEUMONIA BACTERIAL ( 9 FDA reports)
PULMONARY CONGESTION ( 9 FDA reports)
SUBILEUS ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
COORDINATION ABNORMAL ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
GRAFT THROMBOSIS ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
ILEUS PARALYTIC ( 8 FDA reports)
LARGE INTESTINE CARCINOMA ( 8 FDA reports)
LIMB OPERATION ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
SPINAL COMPRESSION FRACTURE ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
TOE AMPUTATION ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
TUMOUR EXCISION ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
BILIARY ANASTOMOSIS ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CHEST X-RAY ABNORMAL ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSLALIA ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ENTEROCOLITIS BACTERIAL ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
INTESTINAL PERFORATION ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
SCHIZOPHRENIA ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
STOMACH DISCOMFORT ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
ATAXIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BREAST DISCOMFORT ( 6 FDA reports)
BREAST PAIN ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
FAECES HARD ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
ORAL INTAKE REDUCED ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
PSYCHIATRIC SYMPTOM ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
THREATENED LABOUR ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
GAZE PALSY ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
MENINGEAL NEOPLASM ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MONONEUROPATHY MULTIPLEX ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 5 FDA reports)
PULMONARY TUBERCULOSIS ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
STUPOR ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
WATER INTOXICATION ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATONIC SEIZURES ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLITIS EROSIVE ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DIABETIC VASCULAR DISORDER ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYDROCELE ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PAPILLOMA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DNA ANTIBODY POSITIVE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMPLANT SITE EXTRAVASATION ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PITUITARY CYST ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
PYOMETRA ( 3 FDA reports)
RECTAL PERFORATION ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL ISCHAEMIA ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VOLUME BLOOD DECREASED ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORTISOL FREE URINE DECREASED ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CSF PROTEIN ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYST ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENDOTOXIC SHOCK ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLAVOBACTERIUM TEST POSITIVE ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYDROXYCORTICOSTEROIDS URINE DECREASED ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONSILLITIS ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL VEIN FLOW DECREASED ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYURIA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL DEPIGMENTATION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOENTERIC FISTULA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD OSMOLARITY ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAMNESIA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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