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

ANAEMIA ( 574 FDA reports)
HAEMATOMA ( 542 FDA reports)
HAEMOGLOBIN DECREASED ( 407 FDA reports)
PULMONARY EMBOLISM ( 400 FDA reports)
HAEMORRHAGE ( 316 FDA reports)
DEEP VEIN THROMBOSIS ( 273 FDA reports)
PYREXIA ( 265 FDA reports)
OFF LABEL USE ( 244 FDA reports)
DYSPNOEA ( 235 FDA reports)
DRUG INEFFECTIVE ( 234 FDA reports)
MUSCLE HAEMORRHAGE ( 223 FDA reports)
VOMITING ( 204 FDA reports)
ABDOMINAL PAIN ( 201 FDA reports)
CEREBRAL HAEMORRHAGE ( 199 FDA reports)
THROMBOCYTOPENIA ( 199 FDA reports)
DEATH ( 197 FDA reports)
OEDEMA PERIPHERAL ( 195 FDA reports)
PAIN ( 192 FDA reports)
PAIN IN EXTREMITY ( 191 FDA reports)
MELAENA ( 174 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 173 FDA reports)
NAUSEA ( 170 FDA reports)
FALL ( 168 FDA reports)
HYPOTENSION ( 164 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 160 FDA reports)
DIARRHOEA ( 158 FDA reports)
RENAL FAILURE ( 146 FDA reports)
SHOCK HAEMORRHAGIC ( 143 FDA reports)
RENAL FAILURE ACUTE ( 141 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 135 FDA reports)
THROMBOSIS ( 135 FDA reports)
OVERDOSE ( 129 FDA reports)
CHEST PAIN ( 127 FDA reports)
PLATELET COUNT DECREASED ( 120 FDA reports)
ARTHRALGIA ( 117 FDA reports)
MALAISE ( 116 FDA reports)
DRUG INTERACTION ( 115 FDA reports)
ASTHENIA ( 112 FDA reports)
SUBDURAL HAEMATOMA ( 110 FDA reports)
HAEMATEMESIS ( 109 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 105 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 105 FDA reports)
CONFUSIONAL STATE ( 102 FDA reports)
PLEURAL EFFUSION ( 99 FDA reports)
BACK PAIN ( 98 FDA reports)
EPISTAXIS ( 97 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 94 FDA reports)
DEHYDRATION ( 93 FDA reports)
COMA ( 91 FDA reports)
DIZZINESS ( 90 FDA reports)
HAEMATOCRIT DECREASED ( 90 FDA reports)
PRODUCT QUALITY ISSUE ( 90 FDA reports)
PALLOR ( 88 FDA reports)
HEADACHE ( 84 FDA reports)
RESPIRATORY FAILURE ( 83 FDA reports)
POST PROCEDURAL HAEMATOMA ( 82 FDA reports)
ANXIETY ( 81 FDA reports)
CONTUSION ( 81 FDA reports)
PNEUMONIA ( 79 FDA reports)
RASH ( 78 FDA reports)
FATIGUE ( 76 FDA reports)
HYPOAESTHESIA ( 76 FDA reports)
SHOCK ( 76 FDA reports)
WEIGHT DECREASED ( 75 FDA reports)
DECREASED APPETITE ( 74 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 72 FDA reports)
URINARY TRACT INFECTION ( 72 FDA reports)
CEREBROVASCULAR ACCIDENT ( 71 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 70 FDA reports)
PLATELET COUNT INCREASED ( 70 FDA reports)
HAEMATURIA ( 69 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 69 FDA reports)
SEPSIS ( 69 FDA reports)
INJECTION SITE PAIN ( 68 FDA reports)
BLOOD CREATININE INCREASED ( 67 FDA reports)
ERYTHEMA ( 65 FDA reports)
INJECTION SITE HAEMATOMA ( 65 FDA reports)
NEUTROPENIA ( 65 FDA reports)
TACHYCARDIA ( 65 FDA reports)
INJURY ( 64 FDA reports)
INFECTION ( 61 FDA reports)
BLOOD PRESSURE DECREASED ( 60 FDA reports)
OSTEOARTHRITIS ( 60 FDA reports)
RESPIRATORY DISTRESS ( 60 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 59 FDA reports)
CEREBRAL HAEMATOMA ( 59 FDA reports)
URTICARIA ( 59 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 58 FDA reports)
RETROPERITONEAL HAEMATOMA ( 58 FDA reports)
HAEMORRHAGIC ANAEMIA ( 56 FDA reports)
MUSCULAR WEAKNESS ( 55 FDA reports)
OSTEONECROSIS OF JAW ( 55 FDA reports)
PRURITUS ( 55 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 54 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 54 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 54 FDA reports)
INFLAMMATION ( 53 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 53 FDA reports)
LYMPHADENOPATHY ( 52 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 52 FDA reports)
GASTRIC ULCER ( 51 FDA reports)
CHILLS ( 50 FDA reports)
SEPTIC SHOCK ( 50 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 49 FDA reports)
CARDIAC ARREST ( 49 FDA reports)
APHASIA ( 48 FDA reports)
HEMIPLEGIA ( 48 FDA reports)
HIATUS HERNIA ( 48 FDA reports)
HYPERTENSION ( 48 FDA reports)
SOMNOLENCE ( 48 FDA reports)
SWELLING ( 48 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 47 FDA reports)
HYPONATRAEMIA ( 47 FDA reports)
INCORRECT DOSE ADMINISTERED ( 47 FDA reports)
LUNG INFILTRATION ( 47 FDA reports)
MULTI-ORGAN FAILURE ( 47 FDA reports)
NECK PAIN ( 47 FDA reports)
PANCYTOPENIA ( 47 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 46 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 46 FDA reports)
INSOMNIA ( 46 FDA reports)
COAGULOPATHY ( 45 FDA reports)
DRY MOUTH ( 45 FDA reports)
EMOTIONAL DISTRESS ( 45 FDA reports)
NEOPLASM MALIGNANT ( 45 FDA reports)
RECTAL HAEMORRHAGE ( 45 FDA reports)
ABDOMINAL PAIN UPPER ( 44 FDA reports)
OEDEMA ( 44 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 44 FDA reports)
CONVULSION ( 43 FDA reports)
MYOCARDIAL INFARCTION ( 43 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 43 FDA reports)
PULMONARY OEDEMA ( 43 FDA reports)
SKIN NECROSIS ( 43 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 42 FDA reports)
BLOOD UREA INCREASED ( 42 FDA reports)
FEMUR FRACTURE ( 42 FDA reports)
HIP FRACTURE ( 42 FDA reports)
HYPERSENSITIVITY ( 42 FDA reports)
LEUKOPENIA ( 42 FDA reports)
PARAESTHESIA ( 42 FDA reports)
DYSPEPSIA ( 41 FDA reports)
DYSPHAGIA ( 41 FDA reports)
LOSS OF CONSCIOUSNESS ( 41 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 40 FDA reports)
HYPOKALAEMIA ( 40 FDA reports)
INCISION SITE HAEMORRHAGE ( 40 FDA reports)
RHABDOMYOLYSIS ( 40 FDA reports)
ACCIDENTAL OVERDOSE ( 39 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 39 FDA reports)
GROIN PAIN ( 39 FDA reports)
PURPURA ( 39 FDA reports)
TRANSAMINASES INCREASED ( 39 FDA reports)
CIRCULATORY COLLAPSE ( 38 FDA reports)
GASTRITIS ( 38 FDA reports)
RASH MACULO-PAPULAR ( 38 FDA reports)
ATRIAL FIBRILLATION ( 37 FDA reports)
DEFORMITY ( 37 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 37 FDA reports)
HAEMOPTYSIS ( 37 FDA reports)
JOINT SWELLING ( 37 FDA reports)
PAIN IN JAW ( 37 FDA reports)
CONDITION AGGRAVATED ( 36 FDA reports)
HEPATIC ENZYME INCREASED ( 36 FDA reports)
PHLEBITIS ( 36 FDA reports)
SPINAL OSTEOARTHRITIS ( 36 FDA reports)
HAEMOLYTIC ANAEMIA ( 35 FDA reports)
JOINT EFFUSION ( 35 FDA reports)
LEUKOCYTOSIS ( 35 FDA reports)
MITRAL VALVE INCOMPETENCE ( 35 FDA reports)
BONE DISORDER ( 34 FDA reports)
HYPOVOLAEMIC SHOCK ( 34 FDA reports)
METASTASES TO LIVER ( 34 FDA reports)
MOBILITY DECREASED ( 34 FDA reports)
MOUTH ULCERATION ( 34 FDA reports)
PALPITATIONS ( 34 FDA reports)
COUGH ( 33 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 33 FDA reports)
HYPERKALAEMIA ( 33 FDA reports)
INTENTIONAL DRUG MISUSE ( 33 FDA reports)
LUNG DISORDER ( 33 FDA reports)
MUSCULOSKELETAL PAIN ( 33 FDA reports)
PARALYSIS ( 33 FDA reports)
RENAL IMPAIRMENT ( 33 FDA reports)
CARDIO-RESPIRATORY ARREST ( 32 FDA reports)
DISEASE PROGRESSION ( 32 FDA reports)
DUODENAL ULCER ( 32 FDA reports)
EYE PAIN ( 32 FDA reports)
FAECES DISCOLOURED ( 32 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 32 FDA reports)
HAEMORRHOIDS ( 32 FDA reports)
METASTASES TO LUNG ( 32 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 32 FDA reports)
TRAUMATIC HAEMATOMA ( 32 FDA reports)
CELLULITIS ( 31 FDA reports)
CEREBRAL INFARCTION ( 31 FDA reports)
HAEMARTHROSIS ( 31 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 31 FDA reports)
OXYGEN SATURATION DECREASED ( 31 FDA reports)
SINUS HEADACHE ( 31 FDA reports)
ANURIA ( 30 FDA reports)
ATELECTASIS ( 30 FDA reports)
BLOOD BILIRUBIN INCREASED ( 30 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 30 FDA reports)
DISORIENTATION ( 30 FDA reports)
EOSINOPHILIA ( 30 FDA reports)
GLOSSITIS ( 30 FDA reports)
IRRITABLE BOWEL SYNDROME ( 30 FDA reports)
MYALGIA ( 30 FDA reports)
NEURALGIA ( 30 FDA reports)
SPINAL COLUMN STENOSIS ( 30 FDA reports)
SYNOVIAL CYST ( 30 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 30 FDA reports)
CARDIAC FAILURE ( 29 FDA reports)
CHONDROMALACIA ( 29 FDA reports)
COLITIS ( 29 FDA reports)
EYE INFECTION ( 29 FDA reports)
FACIAL BONES FRACTURE ( 29 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 29 FDA reports)
HAND FRACTURE ( 29 FDA reports)
HYPERKERATOSIS ( 29 FDA reports)
HYPERTONIC BLADDER ( 29 FDA reports)
MULTIPLE MYELOMA ( 29 FDA reports)
MUSCLE SPASMS ( 29 FDA reports)
SCOLIOSIS ( 29 FDA reports)
SKIN DISCOLOURATION ( 29 FDA reports)
SLEEP APNOEA SYNDROME ( 29 FDA reports)
STAPHYLOCOCCAL INFECTION ( 29 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 29 FDA reports)
THROMBOCYTHAEMIA ( 29 FDA reports)
TONGUE ULCERATION ( 29 FDA reports)
URINARY RETENTION ( 29 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
ASPIRATION ( 28 FDA reports)
GASTRIC HAEMORRHAGE ( 28 FDA reports)
HEPATIC FAILURE ( 28 FDA reports)
HYPOXIA ( 28 FDA reports)
ECCHYMOSIS ( 27 FDA reports)
EMBOLISM ( 27 FDA reports)
GAIT DISTURBANCE ( 27 FDA reports)
LIVER DISORDER ( 27 FDA reports)
SENSORY LOSS ( 27 FDA reports)
ASCITES ( 26 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 26 FDA reports)
DISTURBANCE IN ATTENTION ( 26 FDA reports)
HEPATOCELLULAR INJURY ( 26 FDA reports)
INCISION SITE HAEMATOMA ( 26 FDA reports)
NEURITIS ( 26 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 26 FDA reports)
ASTHMA ( 25 FDA reports)
DYSARTHRIA ( 25 FDA reports)
HEMIPARESIS ( 25 FDA reports)
INTESTINAL ISCHAEMIA ( 25 FDA reports)
MYDRIASIS ( 25 FDA reports)
PROTEIN TOTAL DECREASED ( 25 FDA reports)
SCIATICA ( 25 FDA reports)
DIVERTICULUM ( 24 FDA reports)
DRUG ADMINISTRATION ERROR ( 24 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 24 FDA reports)
HYPERHIDROSIS ( 24 FDA reports)
INJECTION SITE HAEMORRHAGE ( 24 FDA reports)
INTESTINAL OBSTRUCTION ( 24 FDA reports)
MENISCUS LESION ( 24 FDA reports)
RASH ERYTHEMATOUS ( 24 FDA reports)
SPEECH DISORDER ( 24 FDA reports)
ADRENAL INSUFFICIENCY ( 23 FDA reports)
BRAIN HERNIATION ( 23 FDA reports)
BREAST CANCER RECURRENT ( 23 FDA reports)
BURSITIS ( 23 FDA reports)
COMPARTMENT SYNDROME ( 23 FDA reports)
CONSTIPATION ( 23 FDA reports)
HEPATIC CYST ( 23 FDA reports)
MENTAL STATUS CHANGES ( 23 FDA reports)
VASCULAR OCCLUSION ( 23 FDA reports)
VENOUS THROMBOSIS LIMB ( 23 FDA reports)
WOUND HAEMORRHAGE ( 23 FDA reports)
ABDOMINAL DISTENSION ( 22 FDA reports)
BRAIN OEDEMA ( 22 FDA reports)
CYTOLYTIC HEPATITIS ( 22 FDA reports)
GENITAL HERPES ( 22 FDA reports)
INJECTION SITE SWELLING ( 22 FDA reports)
INTERSTITIAL LUNG DISEASE ( 22 FDA reports)
LOCAL SWELLING ( 22 FDA reports)
LYMPHOPENIA ( 22 FDA reports)
PERITONEAL HAEMORRHAGE ( 22 FDA reports)
PNEUMOTHORAX ( 22 FDA reports)
THROMBOCYTOSIS ( 22 FDA reports)
ADRENAL HAEMORRHAGE ( 21 FDA reports)
ADVERSE EVENT ( 21 FDA reports)
AMNESIA ( 21 FDA reports)
ANGINA PECTORIS ( 21 FDA reports)
CHROMATURIA ( 21 FDA reports)
CYSTITIS ( 21 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 21 FDA reports)
GINGIVAL BLEEDING ( 21 FDA reports)
HAEMORRHAGIC STROKE ( 21 FDA reports)
HYPOALBUMINAEMIA ( 21 FDA reports)
JAUNDICE ( 21 FDA reports)
ODYNOPHAGIA ( 21 FDA reports)
PERITONITIS ( 21 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 21 FDA reports)
TREMOR ( 21 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 20 FDA reports)
BLOOD PRESSURE INCREASED ( 20 FDA reports)
CHOLESTASIS ( 20 FDA reports)
EARLY SATIETY ( 20 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 20 FDA reports)
EXTRADURAL HAEMATOMA ( 20 FDA reports)
FLATULENCE ( 20 FDA reports)
HAEMATOCHEZIA ( 20 FDA reports)
HYPERTHERMIA ( 20 FDA reports)
HYPOVOLAEMIA ( 20 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 20 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 20 FDA reports)
MONOPLEGIA ( 20 FDA reports)
NERVOUS SYSTEM DISORDER ( 20 FDA reports)
POST PROCEDURAL COMPLICATION ( 20 FDA reports)
STOMATITIS ( 20 FDA reports)
ANOREXIA ( 19 FDA reports)
BRADYCARDIA ( 19 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
CYANOSIS ( 19 FDA reports)
IMPAIRED HEALING ( 19 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 19 FDA reports)
SKIN DISORDER ( 19 FDA reports)
VENTRICULAR TACHYCARDIA ( 19 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 19 FDA reports)
BLISTER ( 18 FDA reports)
ILL-DEFINED DISORDER ( 18 FDA reports)
INDURATION ( 18 FDA reports)
MEDICATION ERROR ( 18 FDA reports)
NERVE COMPRESSION ( 18 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
PROTEINURIA ( 18 FDA reports)
PROTHROMBIN TIME PROLONGED ( 18 FDA reports)
RASH PRURITIC ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
SYNCOPE ( 18 FDA reports)
TOXIC SKIN ERUPTION ( 18 FDA reports)
UNDERDOSE ( 18 FDA reports)
URETHRAL STENOSIS ( 18 FDA reports)
VENOUS THROMBOSIS ( 18 FDA reports)
BLADDER OPERATION ( 17 FDA reports)
DRUG LEVEL INCREASED ( 17 FDA reports)
FACE OEDEMA ( 17 FDA reports)
FIBRIN D DIMER INCREASED ( 17 FDA reports)
HAEMODYNAMIC INSTABILITY ( 17 FDA reports)
HYPOTHERMIA ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
PANCREATIC CARCINOMA ( 17 FDA reports)
SKIN HAEMORRHAGE ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
WOUND COMPLICATION ( 17 FDA reports)
FEELING HOT ( 16 FDA reports)
HYPERCALCAEMIA ( 16 FDA reports)
INCONTINENCE ( 16 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 16 FDA reports)
LOBAR PNEUMONIA ( 16 FDA reports)
LUNG NEOPLASM ( 16 FDA reports)
LUNG NEOPLASM MALIGNANT ( 16 FDA reports)
MOTOR DYSFUNCTION ( 16 FDA reports)
PULMONARY HAEMORRHAGE ( 16 FDA reports)
RASH GENERALISED ( 16 FDA reports)
RASH MACULAR ( 16 FDA reports)
RESPIRATORY ARREST ( 16 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 16 FDA reports)
URINE COLOUR ABNORMAL ( 16 FDA reports)
ABDOMINAL PAIN LOWER ( 15 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 15 FDA reports)
CHEST WALL MASS ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DRUG HYPERSENSITIVITY ( 15 FDA reports)
EAR PAIN ( 15 FDA reports)
EATING DISORDER ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
FOOT DEFORMITY ( 15 FDA reports)
HYPOMANIA ( 15 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 15 FDA reports)
LUNG INFECTION ( 15 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 15 FDA reports)
MAJOR DEPRESSION ( 15 FDA reports)
NEPHROLITHIASIS ( 15 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 15 FDA reports)
OPERATIVE HAEMORRHAGE ( 15 FDA reports)
PARESIS ( 15 FDA reports)
POLYPECTOMY ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
SINUSITIS ( 15 FDA reports)
SUPERINFECTION ( 15 FDA reports)
TACHYPNOEA ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
ABSCESS ( 14 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
BLOOD BLISTER ( 14 FDA reports)
BONE LESION ( 14 FDA reports)
CATHETER THROMBOSIS ( 14 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
EMPHYSEMA ( 14 FDA reports)
HAEMATOMA INFECTION ( 14 FDA reports)
HAEMOLYSIS ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 14 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 14 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 14 FDA reports)
METRORRHAGIA ( 14 FDA reports)
NECROSIS ( 14 FDA reports)
PETECHIAE ( 14 FDA reports)
POST PROCEDURAL SWELLING ( 14 FDA reports)
PULMONARY FIBROSIS ( 14 FDA reports)
RASH MORBILLIFORM ( 14 FDA reports)
SURGERY ( 14 FDA reports)
THROMBOPHLEBITIS ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
AORTIC VALVE INCOMPETENCE ( 13 FDA reports)
ARTHROPATHY ( 13 FDA reports)
BLOOD ALBUMIN DECREASED ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
BONE PAIN ( 13 FDA reports)
BRONCHIECTASIS ( 13 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 13 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
HAEMORRHAGIC DISORDER ( 13 FDA reports)
HAEMOTHORAX ( 13 FDA reports)
INJECTION SITE BRUISING ( 13 FDA reports)
LUMBAR SPINAL STENOSIS ( 13 FDA reports)
PERICARDIAL EFFUSION ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
SKIN ULCER ( 13 FDA reports)
SPONTANEOUS HAEMATOMA ( 13 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 13 FDA reports)
URINARY INCONTINENCE ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
WOUND SECRETION ( 13 FDA reports)
ABDOMINAL HERNIA ( 12 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 12 FDA reports)
AGITATION ( 12 FDA reports)
ARTHRITIS BACTERIAL ( 12 FDA reports)
BRONCHITIS ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
DERMAL CYST ( 12 FDA reports)
DRUG ERUPTION ( 12 FDA reports)
DYSURIA ( 12 FDA reports)
FLANK PAIN ( 12 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
HEPATIC HAEMORRHAGE ( 12 FDA reports)
HEPATIC LESION ( 12 FDA reports)
HEPATOCELLULAR DAMAGE ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INJECTION SITE ERYTHEMA ( 12 FDA reports)
INJECTION SITE REACTION ( 12 FDA reports)
INTRACRANIAL HAEMATOMA ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
OLIGURIA ( 12 FDA reports)
OSTEITIS ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
OSTEOPENIA ( 12 FDA reports)
PEPTIC ULCER ( 12 FDA reports)
PNEUMONITIS ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
PYURIA ( 12 FDA reports)
RHEUMATOID ARTHRITIS ( 12 FDA reports)
SINUS DISORDER ( 12 FDA reports)
SPINAL LAMINECTOMY ( 12 FDA reports)
SPLENIC HAEMORRHAGE ( 12 FDA reports)
VAGINAL HAEMORRHAGE ( 12 FDA reports)
WALKING AID USER ( 12 FDA reports)
WOUND INFECTION ( 12 FDA reports)
AGRANULOCYTOSIS ( 11 FDA reports)
ARTHRITIS ( 11 FDA reports)
ARTHROPOD BITE ( 11 FDA reports)
BONE MARROW FAILURE ( 11 FDA reports)
BULLOUS LUNG DISEASE ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
FISTULA ( 11 FDA reports)
GASTROINTESTINAL ULCER ( 11 FDA reports)
HEART RATE DECREASED ( 11 FDA reports)
HEPATITIS ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
HYPOCALCAEMIA ( 11 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 11 FDA reports)
INJECTION SITE IRRITATION ( 11 FDA reports)
INTESTINAL PERFORATION ( 11 FDA reports)
LIMB DISCOMFORT ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
METASTASES TO BONE ( 11 FDA reports)
MIGRAINE ( 11 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 11 FDA reports)
PARAPLEGIA ( 11 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 11 FDA reports)
PLEURISY ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
ABDOMINAL TENDERNESS ( 10 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 10 FDA reports)
ANAEMIA POSTOPERATIVE ( 10 FDA reports)
ARTERIAL HAEMORRHAGE ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 10 FDA reports)
CARDIOGENIC SHOCK ( 10 FDA reports)
CATARACT ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DYSPHEMIA ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
EPIGASTRIC DISCOMFORT ( 10 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 10 FDA reports)
EXOSTOSIS ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FOOT FRACTURE ( 10 FDA reports)
GENERALISED OEDEMA ( 10 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 10 FDA reports)
HEART RATE IRREGULAR ( 10 FDA reports)
HYDROCELE ( 10 FDA reports)
HYDROCEPHALUS ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 10 FDA reports)
ISCHAEMIC STROKE ( 10 FDA reports)
JAW OPERATION ( 10 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 10 FDA reports)
LIVE BIRTH ( 10 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MONOPARESIS ( 10 FDA reports)
NERVE ROOT COMPRESSION ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
ORAL PAIN ( 10 FDA reports)
ORTHOSTATIC HYPOTENSION ( 10 FDA reports)
OSTEOLYSIS ( 10 FDA reports)
PELVIC FRACTURE ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PROCEDURAL PAIN ( 10 FDA reports)
PSEUDOMONAL SEPSIS ( 10 FDA reports)
SARCOIDOSIS ( 10 FDA reports)
SPINAL HAEMATOMA ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
STREPTOCOCCAL SEPSIS ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
VASCULAR CALCIFICATION ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
ADENOCARCINOMA ( 9 FDA reports)
BRAIN STEM HAEMORRHAGE ( 9 FDA reports)
BREAST HAEMATOMA ( 9 FDA reports)
BRONCHIOLITIS ( 9 FDA reports)
CARDIOMYOPATHY ( 9 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CEREBELLAR HAEMORRHAGE ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 9 FDA reports)
FAILURE TO THRIVE ( 9 FDA reports)
FLUID RETENTION ( 9 FDA reports)
HAEMORRHAGIC DIATHESIS ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPERCHOLESTEROLAEMIA ( 9 FDA reports)
HYPERPROTEINAEMIA ( 9 FDA reports)
INJECTION SITE URTICARIA ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
MYOPERICARDITIS ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
POLYP COLORECTAL ( 9 FDA reports)
PREMATURE LABOUR ( 9 FDA reports)
RALES ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 9 FDA reports)
RHINITIS ALLERGIC ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
TUMOUR MARKER INCREASED ( 9 FDA reports)
WOUND ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ANHEDONIA ( 8 FDA reports)
BASAL CELL CARCINOMA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CEREBRAL ISCHAEMIA ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 8 FDA reports)
COAGULATION TIME PROLONGED ( 8 FDA reports)
CYSTITIS INTERSTITIAL ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
DIVERTICULUM INTESTINAL ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
FAECALOMA ( 8 FDA reports)
GANGRENE ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEAD INJURY ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
HYPERAESTHESIA ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
ISCHAEMIA ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LIVER INJURY ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
PELVIC HAEMATOMA ( 8 FDA reports)
PERIPHERAL COLDNESS ( 8 FDA reports)
PHYSICAL DISABILITY ( 8 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
POSTOPERATIVE THROMBOSIS ( 8 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 8 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 8 FDA reports)
SPINAL CORD COMPRESSION ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
VASCULITIS ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ACCIDENTAL NEEDLE STICK ( 7 FDA reports)
AGGRESSION ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 7 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
BLADDER DISORDER ( 7 FDA reports)
BLOOD DISORDER ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CARDIAC TAMPONADE ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
FOREIGN BODY ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMANGIOMA ( 7 FDA reports)
HAEMORRHAGIC ASCITES ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPERCOAGULATION ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
HYPOREFLEXIA ( 7 FDA reports)
ILEUS ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
JUGULAR VEIN THROMBOSIS ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
LOW TURNOVER OSTEOPATHY ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
PERITONEAL HAEMATOMA ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
POST PROCEDURAL DRAINAGE ( 7 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
STRESS ( 7 FDA reports)
SUBDURAL HAEMORRHAGE ( 7 FDA reports)
TENDON DISORDER ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
VARICOSE VEIN RUPTURED ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CEREBELLAR HAEMATOMA ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
FEAR ( 6 FDA reports)
HYPERLACTACIDAEMIA ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INCORRECT STORAGE OF DRUG ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MYOCARDIAL STRAIN ( 6 FDA reports)
MYOCARDITIS ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
OESOPHAGEAL ULCER ( 6 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
POLYP ( 6 FDA reports)
POST PROCEDURAL INFECTION ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL HAEMATOMA ( 6 FDA reports)
STRESS ULCER ( 6 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
T-CELL LYMPHOMA ( 6 FDA reports)
ULCER ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
ABDOMINAL HAEMATOMA ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
COAGULATION FACTOR DECREASED ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
COLONIC HAEMATOMA ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERAMYLASAEMIA ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INJECTION SITE DISCOLOURATION ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INJECTION SITE PRURITUS ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INJECTION SITE VESICLES ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
MENISCUS REMOVAL ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NASAL SEPTUM DISORDER ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
OPEN REDUCTION OF FRACTURE ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PERIRENAL HAEMATOMA ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCIATIC NERVE PALSY ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VASCULITIS NECROTISING ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 4 FDA reports)
ACCIDENT ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CATHETER SITE DISCHARGE ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COAGULATION FACTOR X LEVEL ABNORMAL ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 4 FDA reports)
CONJUNCTIVAL PALLOR ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EMBOLISM VENOUS ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FAILURE TO ANASTOMOSE ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 4 FDA reports)
HEPATIC HAEMATOMA ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPOACUSIS ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
HYPOPHYSITIS ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MENINGORRHAGIA ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 4 FDA reports)
SALIVARY GLAND PAIN ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 4 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 4 FDA reports)
SPINAL HAEMANGIOMA ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRACHEAL FISTULA ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 3 FDA reports)
ADACTYLY ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANOREXIA NERVOSA ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHEST WALL OPERATION ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONFABULATION ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYST ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 3 FDA reports)
ERYTHEMA INDURATUM ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FAECAL VOMITING ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMOSTASIS ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEPATIC RUPTURE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INFUSION SITE INFLAMMATION ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LISTERIOSIS ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
MASS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PEDAL PULSE ABNORMAL ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERFORATION BILE DUCT ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RASH SCARLATINIFORM ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SPINAL CORD HAEMORRHAGE ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENIC HAEMATOMA ( 3 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SYNDACTYLY ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THYROID HAEMORRHAGE ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
VAGINAL LACERATION ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WOUND DECOMPOSITION ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPLICATION SITE NODULE ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL BRUIT ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHITIS HAEMOPHILUS ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLANGITIS CHRONIC ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL CLEFT HAND ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FIBRIN INCREASED ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEMIPLEGIA TRANSIENT ( 2 FDA reports)
HEPARIN RESISTANCE ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 2 FDA reports)
PARACENTESIS ABDOMEN ABNORMAL ( 2 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 2 FDA reports)
PARANEOPLASTIC ENCEPHALOMYELITIS ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERINEAL FISTULA ( 2 FDA reports)
PICA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PUNCTURE SITE ABSCESS ( 2 FDA reports)
PUNCTURE SITE PAIN ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL SCAN ABNORMAL ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBIN TIME PROLONGED ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSAMINASES DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTI FACTOR IX ANTIBODY NEGATIVE ( 1 FDA reports)
ANTI FACTOR X ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EARLY MENARCHE ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOTOXAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDEMIC PLEURODYNIA ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE, OBSTRUCTIVE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL OEDEMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE CALCIFICATION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
KWASHIORKOR ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC UTERINE CANCER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERINEAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECIPITATE LABOUR ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
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PRURITUS GENITAL ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAN ( 1 FDA reports)
SCAR ( 1 FDA reports)
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SCREAMING ( 1 FDA reports)
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SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
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SKIN NODULE ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT-GRAFT MALFUNCTION ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
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THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
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UROSEPSIS ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMATOMA ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
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VASCULITIC RASH ( 1 FDA reports)
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VASOCONSTRICTION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR DRAINAGE ( 1 FDA reports)
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VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVECTOMY ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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