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

DERMAL CYST ( 14 FDA reports)
PNEUMONIA ( 12 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
FALL ( 9 FDA reports)
PLEURISY ( 9 FDA reports)
RHABDOMYOLYSIS ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
ADHESION ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PSORIATIC ARTHROPATHY ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL GLAND ( 4 FDA reports)
NEOPLASM OF ORBIT ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
MIDDLE LOBE SYNDROME ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRIST SURGERY ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LENS EXTRACTION ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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