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

ANAEMIA ( 61 FDA reports)
PLATELET COUNT INCREASED ( 47 FDA reports)
HYPERGLYCAEMIA ( 46 FDA reports)
DIARRHOEA ( 43 FDA reports)
OEDEMA PERIPHERAL ( 42 FDA reports)
SEPSIS ( 41 FDA reports)
GENERALISED OEDEMA ( 40 FDA reports)
HYPOTENSION ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 39 FDA reports)
ABORTION SPONTANEOUS ( 38 FDA reports)
DIZZINESS ( 38 FDA reports)
MYOCARDIAL INFARCTION ( 38 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 37 FDA reports)
RENAL FAILURE ( 36 FDA reports)
THROMBOCYTOSIS ( 36 FDA reports)
FATIGUE ( 35 FDA reports)
PAIN ( 35 FDA reports)
LOSS OF CONSCIOUSNESS ( 33 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
MOUTH ULCERATION ( 32 FDA reports)
VASCULITIS ( 32 FDA reports)
BONE PAIN ( 31 FDA reports)
PLEURAL EFFUSION ( 31 FDA reports)
SWELLING ( 31 FDA reports)
WEIGHT DECREASED ( 30 FDA reports)
AREFLEXIA ( 29 FDA reports)
ARRHYTHMIA ( 29 FDA reports)
BRAIN OEDEMA ( 29 FDA reports)
CELLULITIS ( 29 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 29 FDA reports)
HAEMOGLOBIN DECREASED ( 29 FDA reports)
MYDRIASIS ( 29 FDA reports)
OXYGEN SATURATION DECREASED ( 29 FDA reports)
SWELLING FACE ( 29 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 29 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 29 FDA reports)
APPENDICITIS ( 28 FDA reports)
APTYALISM ( 28 FDA reports)
ASTHMA ( 28 FDA reports)
BONE DISORDER ( 28 FDA reports)
BONE EROSION ( 28 FDA reports)
BONE FRAGMENTATION ( 28 FDA reports)
BRONCHOPNEUMONIA ( 28 FDA reports)
COLITIS ULCERATIVE ( 28 FDA reports)
DENTAL CARIES ( 28 FDA reports)
ENTERITIS ( 28 FDA reports)
ENTEROCOCCAL INFECTION ( 28 FDA reports)
ESCHERICHIA INFECTION ( 28 FDA reports)
EXOSTOSIS ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
FOOT FRACTURE ( 28 FDA reports)
GINGIVAL INFECTION ( 28 FDA reports)
GINGIVAL PAIN ( 28 FDA reports)
GINGIVAL SWELLING ( 28 FDA reports)
GINGIVITIS ( 28 FDA reports)
HAEMANGIOMA ( 28 FDA reports)
LUNG DISORDER ( 28 FDA reports)
MALOCCLUSION ( 28 FDA reports)
METASTATIC NEOPLASM ( 28 FDA reports)
OLIGURIA ( 28 FDA reports)
OSTEITIS ( 28 FDA reports)
OSTEITIS DEFORMANS ( 28 FDA reports)
OSTEOARTHRITIS ( 28 FDA reports)
OSTEOLYSIS ( 28 FDA reports)
OSTEOMYELITIS ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
OSTEOPOROSIS ( 28 FDA reports)
PAIN IN JAW ( 28 FDA reports)
PELVIC FRACTURE ( 28 FDA reports)
PERIODONTAL DISEASE ( 28 FDA reports)
PERIODONTITIS ( 28 FDA reports)
POOR DENTAL CONDITION ( 28 FDA reports)
PULPITIS DENTAL ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
SPINAL OSTEOARTHRITIS ( 28 FDA reports)
STOMATITIS ( 28 FDA reports)
TOOTH ABSCESS ( 28 FDA reports)
TOOTH DISORDER ( 28 FDA reports)
TOOTH INJURY ( 28 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 28 FDA reports)
UTERINE LEIOMYOMA ( 28 FDA reports)
VENTRICULAR FIBRILLATION ( 28 FDA reports)
WEGENER'S GRANULOMATOSIS ( 28 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 28 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 27 FDA reports)
HUMERUS FRACTURE ( 27 FDA reports)
JOINT DISLOCATION ( 27 FDA reports)
ROTATOR CUFF SYNDROME ( 27 FDA reports)
SCLERODERMA ( 27 FDA reports)
SHOCK ( 27 FDA reports)
CYTOGENETIC ABNORMALITY ( 26 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 25 FDA reports)
VITREOUS DETACHMENT ( 25 FDA reports)
DYSPHAGIA ( 24 FDA reports)
EMBOLISM ARTERIAL ( 24 FDA reports)
NAUSEA ( 24 FDA reports)
OVERDOSE ( 24 FDA reports)
CARDIAC FAILURE ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
LUMBAR SPINAL STENOSIS ( 23 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 23 FDA reports)
PERICARDIAL EFFUSION ( 23 FDA reports)
ARTERITIS ( 22 FDA reports)
BONE DEBRIDEMENT ( 22 FDA reports)
BONE OPERATION ( 22 FDA reports)
CARDIOMYOPATHY ( 22 FDA reports)
DEVICE FAILURE ( 22 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 22 FDA reports)
ENDODONTIC PROCEDURE ( 22 FDA reports)
NASAL CONGESTION ( 22 FDA reports)
SCAB ( 22 FDA reports)
TOOTH EXTRACTION ( 22 FDA reports)
APPENDICECTOMY ( 21 FDA reports)
CARDIOMEGALY ( 21 FDA reports)
MYOCARDIAL ISCHAEMIA ( 21 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 20 FDA reports)
NEUROPATHY PERIPHERAL ( 20 FDA reports)
OSTEONECROSIS OF JAW ( 20 FDA reports)
PYREXIA ( 20 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 20 FDA reports)
BURSITIS ( 19 FDA reports)
ENCEPHALITIS ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
RECTAL HAEMORRHAGE ( 19 FDA reports)
TACHYARRHYTHMIA ( 19 FDA reports)
TORSADE DE POINTES ( 19 FDA reports)
ANAPHYLACTIC REACTION ( 18 FDA reports)
DELIRIUM ( 18 FDA reports)
FOOT DEFORMITY ( 18 FDA reports)
GUILLAIN-BARRE SYNDROME ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 18 FDA reports)
HYPONATRAEMIA ( 18 FDA reports)
HYPOVOLAEMIC SHOCK ( 18 FDA reports)
NEUROGENIC SHOCK ( 18 FDA reports)
RESPIRATORY DEPRESSION ( 18 FDA reports)
SCAN BONE MARROW ABNORMAL ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 18 FDA reports)
VESTIBULAR DISORDER ( 18 FDA reports)
VOMITING ( 18 FDA reports)
ANGINA PECTORIS ( 17 FDA reports)
GASTROENTERITIS ( 17 FDA reports)
MYELODYSPLASTIC SYNDROME ( 17 FDA reports)
OTITIS EXTERNA ( 17 FDA reports)
PALPITATIONS ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
ANXIETY ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
ACCIDENTAL OVERDOSE ( 15 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
DENTAL OPERATION ( 15 FDA reports)
EMBOLISM ( 15 FDA reports)
GASTRODUODENITIS ( 15 FDA reports)
UTERINE ENLARGEMENT ( 15 FDA reports)
DEATH ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
EPISTAXIS ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
DRY MOUTH ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
SENSORY LOSS ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
ANEURYSM RUPTURED ( 10 FDA reports)
ARTHRALGIA ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
COMPLICATION OF PREGNANCY ( 10 FDA reports)
DIVERTICULUM ( 10 FDA reports)
MYELOFIBROSIS ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
STRESS FRACTURE ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ANAPHYLACTOID SHOCK ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
FALL ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
MENINGITIS ( 9 FDA reports)
MENINGITIS NONINFECTIVE ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
LEFT VENTRICULAR FAILURE ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
ABORTION INDUCED ( 7 FDA reports)
ABORTION THREATENED ( 7 FDA reports)
COMPLICATION OF DELIVERY ( 7 FDA reports)
COUGH ( 7 FDA reports)
LABOUR COMPLICATION ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
VASCULITIS CEREBRAL ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
RASH ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ATROPHIE BLANCHE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
HAEMANGIOMA OF LIVER ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULCER ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URETHRAL REPAIR ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SELECTIVE ABORTION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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