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

DRUG INEFFECTIVE ( 130 FDA reports)
PYREXIA ( 94 FDA reports)
PSORIASIS ( 67 FDA reports)
CROHN'S DISEASE ( 66 FDA reports)
ARTHRALGIA ( 64 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 59 FDA reports)
PNEUMONIA ( 57 FDA reports)
RHEUMATOID ARTHRITIS ( 52 FDA reports)
SEPSIS ( 52 FDA reports)
ANAEMIA ( 42 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 41 FDA reports)
PAIN ( 38 FDA reports)
OEDEMA PERIPHERAL ( 36 FDA reports)
PLEURAL EFFUSION ( 34 FDA reports)
DYSPNOEA ( 33 FDA reports)
LEUKOPENIA ( 33 FDA reports)
SARCOIDOSIS ( 33 FDA reports)
WEIGHT DECREASED ( 33 FDA reports)
RASH ( 32 FDA reports)
PSORIATIC ARTHROPATHY ( 31 FDA reports)
THROMBOCYTOPENIA ( 31 FDA reports)
DERMATITIS BULLOUS ( 30 FDA reports)
NAUSEA ( 30 FDA reports)
PANCYTOPENIA ( 30 FDA reports)
TUBERCULOSIS ( 30 FDA reports)
PAIN IN EXTREMITY ( 29 FDA reports)
MULTI-ORGAN FAILURE ( 27 FDA reports)
DEATH ( 26 FDA reports)
DIARRHOEA ( 26 FDA reports)
COUGH ( 25 FDA reports)
HYPERSENSITIVITY ( 24 FDA reports)
RENAL FAILURE ( 23 FDA reports)
SEPTIC SHOCK ( 23 FDA reports)
BACK PAIN ( 22 FDA reports)
HERPES ZOSTER ( 22 FDA reports)
LUPUS-LIKE SYNDROME ( 22 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 22 FDA reports)
DEEP VEIN THROMBOSIS ( 21 FDA reports)
HEADACHE ( 21 FDA reports)
INJECTION SITE PAIN ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
CONDITION AGGRAVATED ( 20 FDA reports)
VOMITING ( 20 FDA reports)
ASTHENIA ( 19 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
CARDIAC FAILURE ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
HODGKIN'S DISEASE ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
INTERSTITIAL LUNG DISEASE ( 18 FDA reports)
MYOCARDIAL INFARCTION ( 18 FDA reports)
OEDEMA ( 18 FDA reports)
RENAL FAILURE ACUTE ( 18 FDA reports)
SPLENECTOMY ( 18 FDA reports)
FISTULA ( 17 FDA reports)
INJECTION SITE ERYTHEMA ( 17 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
BASAL CELL CARCINOMA ( 16 FDA reports)
CARDIAC MURMUR ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
RALES ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 15 FDA reports)
AUTOIMMUNE HEPATITIS ( 15 FDA reports)
BREAST CANCER ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
DISSEMINATED TUBERCULOSIS ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
MALAISE ( 15 FDA reports)
MICROSCOPIC POLYANGIITIS ( 15 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 15 FDA reports)
PETECHIAE ( 15 FDA reports)
PULMONARY EMBOLISM ( 15 FDA reports)
PURPURA ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
CATARACT ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
ESCHERICHIA SEPSIS ( 14 FDA reports)
INFECTION ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PUSTULAR PSORIASIS ( 14 FDA reports)
SKIN EXFOLIATION ( 14 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 14 FDA reports)
CHILLS ( 13 FDA reports)
COLECTOMY ( 13 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 13 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
INFUSION RELATED REACTION ( 13 FDA reports)
INJECTION SITE REACTION ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
PANCREATIC CARCINOMA ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
CANDIDA SEPSIS ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
INJECTION SITE SWELLING ( 12 FDA reports)
LYMPHOMA ( 12 FDA reports)
RETINAL HAEMORRHAGE ( 12 FDA reports)
ARTHRITIS ( 11 FDA reports)
FALL ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 11 FDA reports)
LARGE INTESTINE PERFORATION ( 11 FDA reports)
LUNG NEOPLASM MALIGNANT ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
PERITONEAL TUBERCULOSIS ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
ADENOCARCINOMA ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CANDIDIASIS ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
FEELING OF DESPAIR ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
ABDOMINAL INJURY ( 9 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
ANXIETY ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
HEPATITIS B ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
PERITONITIS BACTERIAL ( 9 FDA reports)
PNEUMONIA FUNGAL ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
SPORTS INJURY ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
CUTANEOUS SARCOIDOSIS ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
EYE PAIN ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
PARADOXICAL DRUG REACTION ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
TUBERCULOUS PLEURISY ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
ABORTION INDUCED ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DIVERTICULITIS ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
GANGLIONEUROMA ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NAIL INFECTION ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
RASH PRURITIC ( 7 FDA reports)
RIB FRACTURE ( 7 FDA reports)
SERUM SICKNESS ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
VISCERAL LEISHMANIASIS ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BLADDER CANCER ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CERVICAL DYSPLASIA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEMYELINATION ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
EYE NAEVUS ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
INJECTION SITE PRURITUS ( 6 FDA reports)
INJURY ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
MENINGITIS TUBERCULOUS ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MULTIPLE FRACTURES ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NORMAL NEWBORN ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
WHIPPLE'S DISEASE ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DERMATITIS PSORIASIFORM ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HILAR LYMPHADENOPATHY ( 5 FDA reports)
HORNER'S SYNDROME ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
MYCOBACTERIAL INFECTION ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PERTUSSIS ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
POSTOPERATIVE ABSCESS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
ANORECTAL STENOSIS ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BIOPSY LIP ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BONE SARCOMA ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
FOETAL MALFORMATION ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HODGKIN'S DISEASE STAGE II ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
ILEECTOMY ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LIVE BIRTH ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PARACOCCIDIOIDES INFECTION ( 4 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
PULMONARY SARCOIDOSIS ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SEROMA ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENCEPHALITIS VIRAL ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
JOINT TUBERCULOSIS ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LYMPH NODE TUBERCULOSIS ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
NODULE ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OCULAR VASCULITIS ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSEUDOLYMPHOMA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL TUBERCULOSIS ( 3 FDA reports)
SALIVARY GLAND ADENOMA ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TRACHEAL OEDEMA ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CERVIX NEOPLASM ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DIGEORGE'S SYNDROME ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORDER OF ORBIT ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALITIS BRAIN STEM ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENCEPHALITIS POST VARICELLA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA MIGRANS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
ILEOCOLECTOMY ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT MELANOMA STAGE I ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGITIS NONINFECTIVE ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MESENTERIC PANNICULITIS ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEURITIS CRANIAL ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROCTOCOLECTOMY ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 2 FDA reports)
PULMONARY TRICHOSPORONOSIS ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL VASCULITIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SYDENHAM'S CHOREA ( 2 FDA reports)
SYNOVECTOMY ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TUBERCULOMA OF CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
TULARAEMIA ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEST NILE VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AMNIOTIC CAVITY DISORDER ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANTI-VGCC ANTIBODY ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CUTANEOUS LEISHMANIASIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER CANCER STAGE IV ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEPROMATOUS LEPROSY ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC CUTANEOUS CROHN'S DISEASE ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE NEOPLASM ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REBOUND PSORIASIS ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SLE ARTHRITIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBACUTE HEPATIC FAILURE ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VULVAL CANCER STAGE I ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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