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

PLATELET COUNT INCREASED ( 49 FDA reports)
FATIGUE ( 48 FDA reports)
PAIN ( 44 FDA reports)
DIARRHOEA ( 43 FDA reports)
OEDEMA PERIPHERAL ( 43 FDA reports)
ANAEMIA ( 40 FDA reports)
RENAL FAILURE ( 40 FDA reports)
PLEURAL EFFUSION ( 37 FDA reports)
STOMATITIS ( 37 FDA reports)
CELLULITIS ( 36 FDA reports)
COLITIS ULCERATIVE ( 36 FDA reports)
SEPSIS ( 36 FDA reports)
SWELLING FACE ( 36 FDA reports)
VASCULITIS ( 36 FDA reports)
APTYALISM ( 35 FDA reports)
BONE DISORDER ( 35 FDA reports)
BONE EROSION ( 35 FDA reports)
DENTAL CARIES ( 35 FDA reports)
DYSPHAGIA ( 35 FDA reports)
EXOSTOSIS ( 35 FDA reports)
GENERALISED OEDEMA ( 35 FDA reports)
GINGIVAL INFECTION ( 35 FDA reports)
GINGIVAL PAIN ( 35 FDA reports)
GINGIVAL SWELLING ( 35 FDA reports)
MOUTH ULCERATION ( 35 FDA reports)
OLIGURIA ( 35 FDA reports)
OSTEOARTHRITIS ( 35 FDA reports)
OSTEOMYELITIS ( 35 FDA reports)
OSTEOPENIA ( 35 FDA reports)
PERIODONTITIS ( 35 FDA reports)
SPINAL OSTEOARTHRITIS ( 35 FDA reports)
SWELLING ( 35 FDA reports)
THROMBOCYTOSIS ( 35 FDA reports)
BONE FRAGMENTATION ( 34 FDA reports)
LUNG DISORDER ( 34 FDA reports)
MALOCCLUSION ( 34 FDA reports)
METASTATIC NEOPLASM ( 34 FDA reports)
OSTEITIS ( 34 FDA reports)
OSTEOLYSIS ( 34 FDA reports)
POOR DENTAL CONDITION ( 34 FDA reports)
TOOTH DISORDER ( 34 FDA reports)
TOOTH INJURY ( 34 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 34 FDA reports)
UTERINE LEIOMYOMA ( 34 FDA reports)
PYREXIA ( 33 FDA reports)
SCLERODERMA ( 33 FDA reports)
APPENDICITIS ( 32 FDA reports)
BONE PAIN ( 32 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 32 FDA reports)
ABDOMINAL PAIN ( 31 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 31 FDA reports)
ESCHERICHIA INFECTION ( 31 FDA reports)
ASTHMA ( 30 FDA reports)
BRONCHOPNEUMONIA ( 30 FDA reports)
ENTEROCOCCAL INFECTION ( 30 FDA reports)
FOOT FRACTURE ( 30 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 30 FDA reports)
HAEMANGIOMA ( 30 FDA reports)
OSTEOPOROSIS ( 30 FDA reports)
PULPITIS DENTAL ( 30 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 30 FDA reports)
TOOTH ABSCESS ( 30 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 30 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 30 FDA reports)
ENDODONTIC PROCEDURE ( 29 FDA reports)
ENTERITIS ( 29 FDA reports)
FACIAL NEURALGIA ( 29 FDA reports)
GINGIVITIS ( 29 FDA reports)
NASAL CONGESTION ( 29 FDA reports)
OSTEITIS DEFORMANS ( 29 FDA reports)
PAIN IN JAW ( 29 FDA reports)
PELVIC FRACTURE ( 29 FDA reports)
PERIODONTAL DISEASE ( 29 FDA reports)
SCAB ( 29 FDA reports)
SINUSITIS ( 29 FDA reports)
TOOTH EXTRACTION ( 29 FDA reports)
WEGENER'S GRANULOMATOSIS ( 29 FDA reports)
HUMERUS FRACTURE ( 28 FDA reports)
JOINT DISLOCATION ( 28 FDA reports)
NAUSEA ( 28 FDA reports)
ROTATOR CUFF SYNDROME ( 28 FDA reports)
VITREOUS DETACHMENT ( 26 FDA reports)
ANXIETY ( 25 FDA reports)
DEVICE FAILURE ( 24 FDA reports)
HYPERGLYCAEMIA ( 24 FDA reports)
LUMBAR SPINAL STENOSIS ( 24 FDA reports)
BONE DEBRIDEMENT ( 23 FDA reports)
BONE OPERATION ( 23 FDA reports)
APPENDICECTOMY ( 22 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 21 FDA reports)
OSTEONECROSIS OF JAW ( 21 FDA reports)
BURSITIS ( 20 FDA reports)
EYE LASER SURGERY ( 20 FDA reports)
FOOT DEFORMITY ( 20 FDA reports)
SCAN BONE MARROW ABNORMAL ( 20 FDA reports)
WEIGHT DECREASED ( 20 FDA reports)
FALL ( 19 FDA reports)
OTITIS EXTERNA ( 18 FDA reports)
RECTAL HAEMORRHAGE ( 18 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
COR PULMONALE CHRONIC ( 16 FDA reports)
DENTAL OPERATION ( 16 FDA reports)
GASTRODUODENITIS ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
UTERINE ENLARGEMENT ( 16 FDA reports)
OSTEONECROSIS ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
SENSORY LOSS ( 14 FDA reports)
DRY MOUTH ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
STRESS FRACTURE ( 10 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 8 FDA reports)
SERUM FERRITIN INCREASED ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
INJURY ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
RASH ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SURGERY ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
DIZZINESS ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
FIBROSIS ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
MYELOFIBROSIS ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
VASCULITIS CEREBRAL ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
DEATH ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
SCAR ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ARTERITIS ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
ORCHIDECTOMY ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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