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

DEATH ( 423 FDA reports)
THROMBOCYTOPENIA ( 382 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 362 FDA reports)
ANAEMIA ( 360 FDA reports)
PANCYTOPENIA ( 352 FDA reports)
NAUSEA ( 342 FDA reports)
PYREXIA ( 319 FDA reports)
DYSPNOEA ( 318 FDA reports)
NEUTROPENIA ( 318 FDA reports)
DIARRHOEA ( 294 FDA reports)
FATIGUE ( 288 FDA reports)
PNEUMONIA ( 266 FDA reports)
DEHYDRATION ( 258 FDA reports)
VOMITING ( 251 FDA reports)
INTERSTITIAL LUNG DISEASE ( 242 FDA reports)
RASH ( 242 FDA reports)
PLATELET COUNT DECREASED ( 229 FDA reports)
PLEURAL EFFUSION ( 211 FDA reports)
RENAL FAILURE ( 207 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 205 FDA reports)
ASTHENIA ( 199 FDA reports)
FEBRILE NEUTROPENIA ( 198 FDA reports)
MUCOSAL INFLAMMATION ( 191 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 169 FDA reports)
CONSTIPATION ( 157 FDA reports)
SEPSIS ( 155 FDA reports)
RENAL FAILURE ACUTE ( 152 FDA reports)
DISEASE PROGRESSION ( 151 FDA reports)
HAEMOGLOBIN DECREASED ( 146 FDA reports)
NEOPLASM PROGRESSION ( 144 FDA reports)
DECREASED APPETITE ( 139 FDA reports)
NEUTROPHIL COUNT DECREASED ( 126 FDA reports)
RESPIRATORY FAILURE ( 124 FDA reports)
HYPOTENSION ( 120 FDA reports)
ABDOMINAL PAIN ( 113 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 113 FDA reports)
OFF LABEL USE ( 112 FDA reports)
PULMONARY EMBOLISM ( 112 FDA reports)
OEDEMA PERIPHERAL ( 109 FDA reports)
LEUKOPENIA ( 108 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 107 FDA reports)
BONE MARROW FAILURE ( 106 FDA reports)
BLOOD CREATININE INCREASED ( 104 FDA reports)
PAIN ( 100 FDA reports)
CONFUSIONAL STATE ( 98 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 95 FDA reports)
SEPTIC SHOCK ( 94 FDA reports)
MYOCARDIAL INFARCTION ( 93 FDA reports)
HAEMOPTYSIS ( 90 FDA reports)
CHEST PAIN ( 89 FDA reports)
INFECTION ( 89 FDA reports)
RENAL IMPAIRMENT ( 86 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 84 FDA reports)
DIZZINESS ( 84 FDA reports)
MALAISE ( 84 FDA reports)
PERICARDIAL EFFUSION ( 84 FDA reports)
ERYTHEMA ( 81 FDA reports)
NEOPLASM MALIGNANT ( 81 FDA reports)
DEEP VEIN THROMBOSIS ( 76 FDA reports)
COUGH ( 74 FDA reports)
ANOREXIA ( 72 FDA reports)
FALL ( 72 FDA reports)
EPISTAXIS ( 71 FDA reports)
WEIGHT DECREASED ( 70 FDA reports)
DYSPHAGIA ( 67 FDA reports)
HEADACHE ( 67 FDA reports)
ATRIAL FIBRILLATION ( 66 FDA reports)
CEREBROVASCULAR ACCIDENT ( 66 FDA reports)
HOSPITALISATION ( 66 FDA reports)
ALOPECIA ( 65 FDA reports)
ILEUS ( 65 FDA reports)
CARDIAC FAILURE ( 63 FDA reports)
LUNG DISORDER ( 63 FDA reports)
BACK PAIN ( 62 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 59 FDA reports)
HYPONATRAEMIA ( 59 FDA reports)
TACHYCARDIA ( 59 FDA reports)
ARTHRALGIA ( 58 FDA reports)
PRURITUS ( 58 FDA reports)
MUSCULOSKELETAL PAIN ( 57 FDA reports)
STOMATITIS ( 57 FDA reports)
BLOOD PRESSURE DECREASED ( 56 FDA reports)
PNEUMONITIS ( 56 FDA reports)
CARDIO-RESPIRATORY ARREST ( 54 FDA reports)
CONVULSION ( 54 FDA reports)
CELLULITIS ( 53 FDA reports)
HAEMATOCRIT DECREASED ( 53 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 52 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 50 FDA reports)
CHILLS ( 50 FDA reports)
DEPRESSION ( 50 FDA reports)
PAIN IN EXTREMITY ( 50 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 50 FDA reports)
SYNCOPE ( 50 FDA reports)
CARDIAC ARREST ( 49 FDA reports)
HYPERSENSITIVITY ( 49 FDA reports)
HYPERTENSION ( 49 FDA reports)
BLOOD BILIRUBIN INCREASED ( 48 FDA reports)
MULTI-ORGAN FAILURE ( 48 FDA reports)
NON-SMALL CELL LUNG CANCER ( 48 FDA reports)
CONDITION AGGRAVATED ( 47 FDA reports)
LOSS OF CONSCIOUSNESS ( 47 FDA reports)
PERITONITIS ( 47 FDA reports)
URTICARIA ( 47 FDA reports)
HYPOPHAGIA ( 46 FDA reports)
PULMONARY OEDEMA ( 44 FDA reports)
ASCITES ( 43 FDA reports)
HYPERHIDROSIS ( 43 FDA reports)
NEUROPATHY PERIPHERAL ( 43 FDA reports)
OESOPHAGITIS ( 43 FDA reports)
BLOOD UREA INCREASED ( 42 FDA reports)
HOSPICE CARE ( 42 FDA reports)
INSOMNIA ( 42 FDA reports)
RESPIRATORY DISTRESS ( 42 FDA reports)
RASH PRURITIC ( 41 FDA reports)
RASH ERYTHEMATOUS ( 40 FDA reports)
BLOOD GLUCOSE INCREASED ( 39 FDA reports)
CEREBRAL INFARCTION ( 39 FDA reports)
HAEMORRHAGE ( 39 FDA reports)
HYPOXIA ( 39 FDA reports)
LIVER DISORDER ( 39 FDA reports)
ANXIETY ( 38 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 38 FDA reports)
MENTAL STATUS CHANGES ( 38 FDA reports)
OSTEONECROSIS ( 38 FDA reports)
CARDIAC MURMUR ( 37 FDA reports)
PULMONARY FIBROSIS ( 37 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 37 FDA reports)
ATELECTASIS ( 36 FDA reports)
DIVERTICULITIS ( 36 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 36 FDA reports)
HAEMATOTOXICITY ( 36 FDA reports)
HEPATIC FAILURE ( 36 FDA reports)
HYPOAESTHESIA ( 36 FDA reports)
HYPOKALAEMIA ( 36 FDA reports)
INTESTINAL PERFORATION ( 36 FDA reports)
LUNG NEOPLASM MALIGNANT ( 36 FDA reports)
SOMNOLENCE ( 35 FDA reports)
OEDEMA ( 34 FDA reports)
ANAPHYLACTIC REACTION ( 33 FDA reports)
ANAPHYLACTIC SHOCK ( 33 FDA reports)
BLOOD SODIUM DECREASED ( 33 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 33 FDA reports)
PNEUMONIA ASPIRATION ( 33 FDA reports)
HYPERKALAEMIA ( 32 FDA reports)
METASTASES TO BONE ( 32 FDA reports)
OXYGEN SATURATION DECREASED ( 32 FDA reports)
SHOCK ( 32 FDA reports)
BLOOD ALBUMIN DECREASED ( 31 FDA reports)
DRUG TOXICITY ( 31 FDA reports)
HAEMOLYTIC ANAEMIA ( 31 FDA reports)
SUDDEN DEATH ( 31 FDA reports)
CHOLESTASIS ( 30 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 30 FDA reports)
HYPOCALCAEMIA ( 29 FDA reports)
LUNG INFILTRATION ( 29 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 28 FDA reports)
COLITIS ( 28 FDA reports)
HYDRONEPHROSIS ( 28 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 28 FDA reports)
NEUTROPENIC SEPSIS ( 28 FDA reports)
ORAL CANDIDIASIS ( 28 FDA reports)
PARAESTHESIA ( 28 FDA reports)
ABDOMINAL PAIN UPPER ( 27 FDA reports)
DRUG INEFFECTIVE ( 27 FDA reports)
EMBOLISM ARTERIAL ( 27 FDA reports)
FEBRILE BONE MARROW APLASIA ( 27 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 26 FDA reports)
CYTOLYTIC HEPATITIS ( 26 FDA reports)
DERMATITIS BULLOUS ( 26 FDA reports)
HAEMATURIA ( 26 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 26 FDA reports)
PERFORMANCE STATUS DECREASED ( 26 FDA reports)
PNEUMOTHORAX ( 26 FDA reports)
PURPURA ( 26 FDA reports)
RADIATION PNEUMONITIS ( 26 FDA reports)
VASCULITIS ( 26 FDA reports)
DRUG HYPERSENSITIVITY ( 25 FDA reports)
GAIT DISTURBANCE ( 25 FDA reports)
HAEMATEMESIS ( 25 FDA reports)
HERPES ZOSTER ( 25 FDA reports)
INTESTINAL OBSTRUCTION ( 25 FDA reports)
MEDICATION ERROR ( 25 FDA reports)
TRANSAMINASES INCREASED ( 25 FDA reports)
CONJUNCTIVITIS ( 24 FDA reports)
DERMATITIS ( 24 FDA reports)
DIVERTICULAR PERFORATION ( 24 FDA reports)
GASTROINTESTINAL NECROSIS ( 24 FDA reports)
SKIN EXFOLIATION ( 24 FDA reports)
TOXIC SKIN ERUPTION ( 24 FDA reports)
ABDOMINAL DISTENSION ( 23 FDA reports)
BONE DISORDER ( 23 FDA reports)
CANDIDIASIS ( 23 FDA reports)
COMA ( 23 FDA reports)
LUNG INFECTION ( 23 FDA reports)
MOUTH ULCERATION ( 23 FDA reports)
ANHEDONIA ( 22 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 22 FDA reports)
DYSPNOEA EXERTIONAL ( 22 FDA reports)
FLATULENCE ( 22 FDA reports)
HYPOMAGNESAEMIA ( 22 FDA reports)
RASH GENERALISED ( 22 FDA reports)
RESPIRATORY DISORDER ( 22 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
BLOOD PRESSURE INCREASED ( 21 FDA reports)
BONE PAIN ( 21 FDA reports)
CARDIAC DISORDER ( 21 FDA reports)
CHEST DISCOMFORT ( 21 FDA reports)
GASTRIC ULCER ( 21 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 21 FDA reports)
ISCHAEMIC STROKE ( 21 FDA reports)
OSTEONECROSIS OF JAW ( 21 FDA reports)
PETECHIAE ( 21 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 21 FDA reports)
THROMBOSIS ( 21 FDA reports)
ARTERIOSCLEROSIS ( 20 FDA reports)
CHOLELITHIASIS ( 20 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
ENCEPHALOPATHY ( 20 FDA reports)
FACE OEDEMA ( 20 FDA reports)
GASTRITIS ( 20 FDA reports)
GENERALISED OEDEMA ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
ILEUS PARALYTIC ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 20 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 20 FDA reports)
MELAENA ( 20 FDA reports)
RECALL PHENOMENON ( 20 FDA reports)
RECTAL HAEMORRHAGE ( 20 FDA reports)
SKIN DISCOLOURATION ( 20 FDA reports)
TOOTH ABSCESS ( 20 FDA reports)
ABDOMINAL DISCOMFORT ( 19 FDA reports)
FLUSHING ( 19 FDA reports)
GASTROINTESTINAL PERFORATION ( 19 FDA reports)
HEART RATE INCREASED ( 19 FDA reports)
HYPOALBUMINAEMIA ( 19 FDA reports)
METASTASES TO LIVER ( 19 FDA reports)
NEPHROPATHY TOXIC ( 19 FDA reports)
PANCREATITIS ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
SWELLING ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
WHEEZING ( 19 FDA reports)
BLOOD CALCIUM DECREASED ( 18 FDA reports)
BRONCHOPNEUMONIA ( 18 FDA reports)
CYANOSIS ( 18 FDA reports)
DELIRIUM ( 18 FDA reports)
EJECTION FRACTION DECREASED ( 18 FDA reports)
EMPHYSEMA ( 18 FDA reports)
OESOPHAGEAL ULCER ( 18 FDA reports)
PALPITATIONS ( 18 FDA reports)
PRODUCTIVE COUGH ( 18 FDA reports)
PULMONARY TOXICITY ( 18 FDA reports)
RENAL DISORDER ( 18 FDA reports)
BRONCHOSPASM ( 17 FDA reports)
DISORIENTATION ( 17 FDA reports)
DIVERTICULUM INTESTINAL ( 17 FDA reports)
ENTEROCOLITIS ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
HICCUPS ( 17 FDA reports)
HYPERGLYCAEMIA ( 17 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 17 FDA reports)
JAUNDICE ( 17 FDA reports)
LARGE INTESTINE PERFORATION ( 17 FDA reports)
LYMPHOEDEMA ( 17 FDA reports)
MALNUTRITION ( 17 FDA reports)
METASTASES TO LUNG ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
PERICARDITIS ( 17 FDA reports)
PHLEBITIS ( 17 FDA reports)
PLATELET COUNT INCREASED ( 17 FDA reports)
PULMONARY HYPERTENSION ( 17 FDA reports)
RASH MACULAR ( 17 FDA reports)
SINUS TACHYCARDIA ( 17 FDA reports)
STEVENS-JOHNSON SYNDROME ( 17 FDA reports)
TREMOR ( 17 FDA reports)
ACUTE RESPIRATORY FAILURE ( 16 FDA reports)
BODY TEMPERATURE INCREASED ( 16 FDA reports)
DYSPEPSIA ( 16 FDA reports)
ERYSIPELAS ( 16 FDA reports)
INJURY ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
BLOOD COUNT ABNORMAL ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
NEUROPATHY ( 15 FDA reports)
ORAL PAIN ( 15 FDA reports)
RASH PAPULAR ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
AGITATION ( 14 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 14 FDA reports)
ATRIAL FLUTTER ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
BLOOD URINE PRESENT ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
ECZEMA ( 14 FDA reports)
EMBOLISM ( 14 FDA reports)
EXTREMITY NECROSIS ( 14 FDA reports)
FAILURE TO THRIVE ( 14 FDA reports)
FEMUR FRACTURE ( 14 FDA reports)
HEMIPARESIS ( 14 FDA reports)
IMPAIRED HEALING ( 14 FDA reports)
INFLAMMATION ( 14 FDA reports)
LETHARGY ( 14 FDA reports)
LYMPHADENOPATHY ( 14 FDA reports)
MESOTHELIOMA ( 14 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 14 FDA reports)
PYOTHORAX ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
SKIN TOXICITY ( 14 FDA reports)
TOOTHACHE ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
BACTERIAL INFECTION ( 13 FDA reports)
BURNING SENSATION ( 13 FDA reports)
CEREBRAL HAEMORRHAGE ( 13 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 13 FDA reports)
CONTUSION ( 13 FDA reports)
DYSGEUSIA ( 13 FDA reports)
FEELING HOT ( 13 FDA reports)
HAEMOTHORAX ( 13 FDA reports)
HEPATIC ENZYME INCREASED ( 13 FDA reports)
LACRIMATION INCREASED ( 13 FDA reports)
NECK PAIN ( 13 FDA reports)
PAIN IN JAW ( 13 FDA reports)
PERIPHERAL ISCHAEMIA ( 13 FDA reports)
RIGHT VENTRICULAR FAILURE ( 13 FDA reports)
SWELLING FACE ( 13 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 13 FDA reports)
VAGINAL HAEMORRHAGE ( 13 FDA reports)
ANGIOEDEMA ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
CARDIOMYOPATHY ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
DYSARTHRIA ( 12 FDA reports)
DYSURIA ( 12 FDA reports)
ELECTROLYTE IMBALANCE ( 12 FDA reports)
ENTERITIS ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
HAEMOGLOBIN ABNORMAL ( 12 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
HEPATOCELLULAR INJURY ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
HYPOPROTEINAEMIA ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
ORAL INTAKE REDUCED ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
PERIODONTAL DISEASE ( 12 FDA reports)
PROTHROMBIN TIME PROLONGED ( 12 FDA reports)
PULMONARY MICROEMBOLI ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
FUNGAL INFECTION ( 11 FDA reports)
GASTRITIS EROSIVE ( 11 FDA reports)
GASTROENTERITIS RADIATION ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
ILEAL PERFORATION ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
INGROWING NAIL ( 11 FDA reports)
METASTASIS ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 11 FDA reports)
OBSTRUCTION ( 11 FDA reports)
ORTHOSTATIC HYPOTENSION ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
PERIORBITAL OEDEMA ( 11 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 11 FDA reports)
PLEURITIC PAIN ( 11 FDA reports)
RADICULOPATHY ( 11 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 11 FDA reports)
SMALL INTESTINE ULCER ( 11 FDA reports)
TOOTH LOSS ( 11 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 11 FDA reports)
ABDOMINAL ABSCESS ( 10 FDA reports)
ANAPHYLACTOID REACTION ( 10 FDA reports)
BLOOD MAGNESIUM DECREASED ( 10 FDA reports)
CANCER PAIN ( 10 FDA reports)
CARDIOTOXICITY ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DIABETES INSIPIDUS ( 10 FDA reports)
EPIDERMOLYSIS ( 10 FDA reports)
GROIN PAIN ( 10 FDA reports)
HALLUCINATION, VISUAL ( 10 FDA reports)
HYDROURETER ( 10 FDA reports)
HYPOVOLAEMIA ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
ISCHAEMIC HEPATITIS ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
METASTASES TO LYMPH NODES ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
PROSTATOMEGALY ( 10 FDA reports)
RADIATION OESOPHAGITIS ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
SCLERODERMA ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
SUBILEUS ( 10 FDA reports)
TREATMENT NONCOMPLIANCE ( 10 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
AMNESIA ( 9 FDA reports)
APHASIA ( 9 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BONE EROSION ( 9 FDA reports)
BONE LESION ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CLOSTRIDIAL INFECTION ( 9 FDA reports)
COLD SWEAT ( 9 FDA reports)
DIZZINESS POSTURAL ( 9 FDA reports)
FLUID OVERLOAD ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
GASTROENTERITIS ( 9 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 9 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 9 FDA reports)
HEPATITIS ACUTE ( 9 FDA reports)
HYDROCELE ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
LUNG CANCER METASTATIC ( 9 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MASS ( 9 FDA reports)
MASTICATION DISORDER ( 9 FDA reports)
METASTASES TO MENINGES ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
PARANEOPLASTIC SYNDROME ( 9 FDA reports)
PARONYCHIA ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PRIMARY SEQUESTRUM ( 9 FDA reports)
PROSTATE CANCER METASTATIC ( 9 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RENAL SALT-WASTING SYNDROME ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 9 FDA reports)
SPLEEN DISORDER ( 9 FDA reports)
TESTICULAR PAIN ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
URETERAL NEOPLASM ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
VITAMIN B12 INCREASED ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
ALVEOLITIS ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
BRONCHIAL FISTULA ( 8 FDA reports)
COLITIS ISCHAEMIC ( 8 FDA reports)
COLONIC STENOSIS ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GASTROINTESTINAL TOXICITY ( 8 FDA reports)
HAEMATOCRIT ABNORMAL ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEPATORENAL FAILURE ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
LUNG ADENOCARCINOMA ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
MOUTH HAEMORRHAGE ( 8 FDA reports)
PERICARDITIS URAEMIC ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PRESYNCOPE ( 8 FDA reports)
PROTEIN TOTAL INCREASED ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 8 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 8 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 8 FDA reports)
THROAT TIGHTNESS ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ANAL FISTULA ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
APLASIA ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BONE FRAGMENTATION ( 7 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 7 FDA reports)
BRONCHIAL OBSTRUCTION ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DEFORMITY ( 7 FDA reports)
DENTAL OPERATION ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
ERECTILE DYSFUNCTION ( 7 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
GLOSSITIS ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
HERPES OESOPHAGITIS ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 7 FDA reports)
LUNG ABSCESS ( 7 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 7 FDA reports)
MALOCCLUSION ( 7 FDA reports)
METASTASES TO PERITONEUM ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
PAPILLOEDEMA ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
ROTATOR CUFF SYNDROME ( 7 FDA reports)
SKIN HYPERPIGMENTATION ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
TOOTH DISORDER ( 7 FDA reports)
TUMOUR PAIN ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANURIA ( 6 FDA reports)
APHTHOUS STOMATITIS ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD CREATININE DECREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 6 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CYTOKINE RELEASE SYNDROME ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
HYPOCHOLESTEROLAEMIA ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METASTASES TO ADRENALS ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MUCOSAL HAEMORRHAGE ( 6 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
NEUTROPENIC COLITIS ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
PATHOLOGICAL FRACTURE ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SPLENIC RUPTURE ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ACUTE ABDOMEN ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CAECITIS ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENZYME ABNORMALITY ( 5 FDA reports)
EPILEPSY ( 5 FDA reports)
ERYSIPELOID ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GRANULOCYTE COUNT DECREASED ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
JOINT EFFUSION ( 5 FDA reports)
JOINT SURGERY ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
OSTEOLYSIS ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PLATELET COUNT ABNORMAL ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RETCHING ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ABSCESS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
ECZEMA ASTEATOTIC ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 4 FDA reports)
MESOTHELIOMA MALIGNANT RECURRENT ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OLIGODIPSIA ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERITONEAL DISORDER ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PORTAL VENOUS GAS ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
PULMONARY NECROSIS ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SMALL INTESTINAL PERFORATION ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR DYSKINESIA ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DERMO-HYPODERMITIS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING HOT AND COLD ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LACTOBACILLUS INFECTION ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MILLER FISHER SYNDROME ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEUROSENSORY HYPOACUSIS ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OMENTAL INFARCTION ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
ORAL CAVITY FISTULA ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL INFECTION ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PROCTOCOLITIS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCROTAL GANGRENE ( 3 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPY RESPONDER ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEIGHT FLUCTUATION ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APPLICATION SITE PARAESTHESIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD FOLATE ABNORMAL ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CAMPYLOBACTER INFECTION ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERVICAL ROOT PAIN ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DENTAL DISCOMFORT ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KERATITIS INTERSTITIAL ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MECHANICAL ILEUS ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ADVANCED ( 2 FDA reports)
METASTASES TO MUSCLE ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROPATHIC PAIN ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL FISTULA ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURAL MESOTHELIOMA ( 2 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 2 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT RECURRENT ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIATION INTERACTION ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR LOCAL INVASION ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
ULCER ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AKINAESTHESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL PNEUMONIA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FOLATE ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CREATINE URINE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALITIS PERIAXIALIS DIFFUSA ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOCORTICOIDS DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION RELATED REACTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKAEMIA GRANULOCYTIC ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO DIAPHRAGM ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTASES TO UTERUS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCOAST'S TUMOUR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTIAL LUNG RESECTION ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RADIATION EXPOSURE ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCINTIGRAPHY ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA LOCALISED ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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