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

DRUG INTERACTION ( 132 FDA reports)
PYREXIA ( 128 FDA reports)
NAUSEA ( 81 FDA reports)
FALL ( 79 FDA reports)
PNEUMONIA ( 78 FDA reports)
VOMITING ( 77 FDA reports)
RENAL FAILURE ACUTE ( 70 FDA reports)
HAEMOGLOBIN DECREASED ( 68 FDA reports)
INTERSTITIAL LUNG DISEASE ( 68 FDA reports)
HYPOCALCAEMIA ( 67 FDA reports)
RENAL FAILURE ( 67 FDA reports)
MALAISE ( 65 FDA reports)
BLOOD CREATININE INCREASED ( 61 FDA reports)
PLEURAL EFFUSION ( 57 FDA reports)
SEPSIS ( 57 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 56 FDA reports)
DIARRHOEA ( 56 FDA reports)
RHABDOMYOLYSIS ( 56 FDA reports)
DEATH ( 53 FDA reports)
HYPERCALCAEMIA ( 51 FDA reports)
APLASIA PURE RED CELL ( 50 FDA reports)
ANAEMIA ( 49 FDA reports)
PANCYTOPENIA ( 49 FDA reports)
CONDITION AGGRAVATED ( 48 FDA reports)
URINARY TRACT INFECTION ( 48 FDA reports)
DIZZINESS ( 47 FDA reports)
DEHYDRATION ( 46 FDA reports)
HYPERKALAEMIA ( 45 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 44 FDA reports)
ARTHRALGIA ( 44 FDA reports)
DYSPNOEA ( 44 FDA reports)
RASH ( 44 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 44 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 43 FDA reports)
CARDIAC FAILURE ( 43 FDA reports)
HYPERTENSION ( 43 FDA reports)
HYPOKALAEMIA ( 43 FDA reports)
HYPOTENSION ( 42 FDA reports)
CONFUSIONAL STATE ( 41 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 40 FDA reports)
LIVER DISORDER ( 40 FDA reports)
RENAL FAILURE CHRONIC ( 40 FDA reports)
CARDIAC ARREST ( 38 FDA reports)
CONVULSION ( 38 FDA reports)
DECREASED APPETITE ( 38 FDA reports)
GAIT DISTURBANCE ( 38 FDA reports)
OEDEMA PERIPHERAL ( 38 FDA reports)
RENAL IMPAIRMENT ( 37 FDA reports)
ATRIAL FIBRILLATION ( 36 FDA reports)
HEADACHE ( 36 FDA reports)
ABDOMINAL PAIN ( 35 FDA reports)
LOSS OF CONSCIOUSNESS ( 35 FDA reports)
ASTHENIA ( 34 FDA reports)
CONSTIPATION ( 34 FDA reports)
HYPOMAGNESAEMIA ( 33 FDA reports)
PERITONITIS ( 33 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 32 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 32 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 31 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 31 FDA reports)
RHEUMATOID ARTHRITIS ( 31 FDA reports)
FATIGUE ( 30 FDA reports)
HYPOGLYCAEMIA ( 30 FDA reports)
BACK PAIN ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 28 FDA reports)
HAEMODIALYSIS ( 28 FDA reports)
INFECTION ( 28 FDA reports)
MYOCARDIAL ISCHAEMIA ( 28 FDA reports)
ANOREXIA ( 27 FDA reports)
CHEST PAIN ( 27 FDA reports)
CHILLS ( 26 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 26 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 26 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 25 FDA reports)
BLOOD PRESSURE INCREASED ( 25 FDA reports)
BLOOD UREA INCREASED ( 24 FDA reports)
BRADYCARDIA ( 24 FDA reports)
BRONCHITIS ( 24 FDA reports)
MUSCULAR WEAKNESS ( 24 FDA reports)
PARAESTHESIA ( 24 FDA reports)
RESPIRATORY FAILURE ( 24 FDA reports)
SOMNOLENCE ( 24 FDA reports)
TETANY ( 24 FDA reports)
BLOOD PRESSURE DECREASED ( 23 FDA reports)
LETHARGY ( 23 FDA reports)
NASOPHARYNGITIS ( 23 FDA reports)
FLUID OVERLOAD ( 22 FDA reports)
HAEMATOMA ( 22 FDA reports)
MULTI-ORGAN FAILURE ( 22 FDA reports)
SEPTIC SHOCK ( 22 FDA reports)
CEREBRAL INFARCTION ( 21 FDA reports)
DEEP VEIN THROMBOSIS ( 21 FDA reports)
PAIN IN EXTREMITY ( 21 FDA reports)
SHOCK ( 21 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 20 FDA reports)
BLOOD GLUCOSE INCREASED ( 20 FDA reports)
DEPRESSION ( 20 FDA reports)
HERPES ZOSTER ( 20 FDA reports)
PAIN ( 20 FDA reports)
PANCREATITIS ACUTE ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
COUGH ( 19 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 19 FDA reports)
DIABETES MELLITUS ( 19 FDA reports)
INFLAMMATION ( 19 FDA reports)
OEDEMA ( 19 FDA reports)
PARAPARESIS ( 19 FDA reports)
PROTEINURIA ( 19 FDA reports)
TREMOR ( 19 FDA reports)
TUBERCULOSIS ( 19 FDA reports)
ASPIRATION BONE MARROW ( 18 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 18 FDA reports)
CATARACT ( 18 FDA reports)
CIRCULATORY COLLAPSE ( 18 FDA reports)
FIBULA FRACTURE ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
JOINT STIFFNESS ( 18 FDA reports)
MYOCARDIAL INFARCTION ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
BONE PAIN ( 17 FDA reports)
CARDIO-RESPIRATORY ARREST ( 17 FDA reports)
CELLULITIS ( 17 FDA reports)
DIALYSIS ( 17 FDA reports)
DISORIENTATION ( 17 FDA reports)
DRUG TOXICITY ( 17 FDA reports)
ENCEPHALOPATHY ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 17 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 17 FDA reports)
LEUKOPENIA ( 17 FDA reports)
ORGANISING PNEUMONIA ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
SPINAL COMPRESSION FRACTURE ( 17 FDA reports)
VERTIGO ( 17 FDA reports)
AZOTAEMIA ( 16 FDA reports)
BIOPSY BONE MARROW ( 16 FDA reports)
CALCIPHYLAXIS ( 16 FDA reports)
DELIRIUM ( 16 FDA reports)
FEMUR FRACTURE ( 16 FDA reports)
IRON OVERLOAD ( 16 FDA reports)
JAUNDICE ( 16 FDA reports)
MUSCLE SPASMS ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 15 FDA reports)
HAEMORRHAGE ( 15 FDA reports)
HEAD INJURY ( 15 FDA reports)
RESTLESSNESS ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
VISUAL ACUITY REDUCED ( 15 FDA reports)
AGITATION ( 14 FDA reports)
ARRHYTHMIA ( 14 FDA reports)
COMA ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
HYPOTONIA ( 14 FDA reports)
ILEUS ( 14 FDA reports)
LARGE INTESTINE PERFORATION ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
NEPHROPATHY TOXIC ( 14 FDA reports)
OPTIC DISC DISORDER ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
RENAL TRANSPLANT ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
ACIDOSIS ( 13 FDA reports)
ALOPECIA ( 13 FDA reports)
ASCITES ( 13 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 13 FDA reports)
HEPATIC FAILURE ( 13 FDA reports)
HYPERCAPNIA ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
PLEURAL FIBROSIS ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
VENTRICULAR TACHYCARDIA ( 13 FDA reports)
ABASIA ( 12 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
CARDIAC HYPERTROPHY ( 12 FDA reports)
FULL BLOOD COUNT DECREASED ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
SEROTONIN SYNDROME ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
DRUG LEVEL INCREASED ( 11 FDA reports)
FEMORAL NECK FRACTURE ( 11 FDA reports)
FLUID RETENTION ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
HEPATITIS B ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
INTESTINAL OBSTRUCTION ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
OSTEOARTHRITIS ( 11 FDA reports)
OSTEONECROSIS ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
SINUS TACHYCARDIA ( 11 FDA reports)
STOMATITIS ( 11 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
ARTHRITIS BACTERIAL ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
DRUG ERUPTION ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
PNEUMONIA LEGIONELLA ( 10 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BONE NEOPLASM ( 9 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CHEST X-RAY ABNORMAL ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
FOLLICULAR MUCINOSIS ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
MYOPATHY ( 9 FDA reports)
NEPHROPATHY ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PERITONEAL TUBERCULOSIS ( 9 FDA reports)
PNEUMONIA BACTERIAL ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
PYURIA ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
SPINAL OSTEOARTHRITIS ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
TRANSPLANT REJECTION ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
CARDIAC TAMPONADE ( 8 FDA reports)
DECUBITUS ULCER ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
HYPERPYREXIA ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
LUMBAR SPINAL STENOSIS ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
PURPURA ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
TUBERCULOUS PLEURISY ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ANGIOGRAM ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 7 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 7 FDA reports)
INJECTION SITE INDURATION ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
RETINAL HAEMORRHAGE ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
VENOUS THROMBOSIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ADRENAL ATROPHY ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
AMPUTATION ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
APHASIA ( 6 FDA reports)
APLASTIC ANAEMIA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 6 FDA reports)
BLOOD LACTIC ACID INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
MELAENA ( 6 FDA reports)
NASAL SINUS CANCER ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
OVARIAN NEOPLASM ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SHUNT OCCLUSION ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HEPATITIS B DNA INCREASED ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
INTUSSUSCEPTION ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PERITONEAL DISORDER ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PUBIS FRACTURE ( 5 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 5 FDA reports)
SEROSITIS ( 5 FDA reports)
SHUNT THROMBOSIS ( 5 FDA reports)
SINUS ARREST ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
THIRST ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TUMOUR NECROSIS FACTOR RECEPTOR-ASSOCIATED PERIODIC SYNDROME ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
ANTIBODY TEST ABNORMAL ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSCHEZIA ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
ENDOPHTHALMITIS ( 4 FDA reports)
ENDOTOXIC SHOCK ( 4 FDA reports)
ENTEROCOLITIS BACTERIAL ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
FUNGAL PERITONITIS ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAEMORRHAGIC ASCITES ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATOBLASTOMA ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INFECTED CYST ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MENINGOCOCCAL SEPSIS ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
PYOTHORAX ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
SPUTUM PURULENT ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
AMINOACIDURIA ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BIRTH MARK ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COELIAC ARTERY OCCLUSION ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FRACTURED ISCHIUM ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOCOMPLEMENTAEMIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LENS DISLOCATION ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LUNG CYST ( 3 FDA reports)
LYMPHANGIOMA ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENINGEAL NEOPLASM ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MILK-ALKALI SYNDROME ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PERICARDITIS TUBERCULOUS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SMALL INTESTINE GANGRENE ( 3 FDA reports)
SOFT TISSUE INFLAMMATION ( 3 FDA reports)
SOFT TISSUE NECROSIS ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THERMOHYPOAESTHESIA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TUMOUR EMBOLISM ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
AMPUTATION STUMP PAIN ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID ( 2 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE UNSPECIFIED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE EPIPHYSEAL DYSPLASIA ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSSICLE DISORDER ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PATHOLOGICAL GAMBLING ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECONDARY AMYLOIDOSIS ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VIIITH NERVE INJURY ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTATIN C INCREASED ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHROPLASIA ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOCALCIURIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA OESOPHAGEAL ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC UTERINE CANCER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PEPTOSTREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POCKET EROSION ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL NEOPLASM ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SALT INTOXICATION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON GRAFT ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOLOSA-HUNT SYNDROME ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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