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

PNEUMONIA ( 31 FDA reports)
DYSPNOEA ( 24 FDA reports)
NAUSEA ( 20 FDA reports)
FATIGUE ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 13 FDA reports)
LEUKOPENIA ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
LUNG INFECTION ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
DEATH ( 10 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 10 FDA reports)
PLEURISY ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
PAIN ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
RASH ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
COMA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
VOMITING ( 7 FDA reports)
DEPRESSION ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
SWELLING ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
FALL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
LABYRINTHITIS ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MYOCARDIAL RUPTURE ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MENINGOCOCCAL SEPSIS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG HALF-LIFE INCREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICHOPHYTIC GRANULOMA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VAGINAL FISTULA ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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