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

NAUSEA ( 45 FDA reports)
VOMITING ( 42 FDA reports)
BONE DISORDER ( 32 FDA reports)
PAIN IN JAW ( 32 FDA reports)
FISTULA ( 31 FDA reports)
INJURY ( 31 FDA reports)
PARAESTHESIA ORAL ( 30 FDA reports)
NEUROPATHY PERIPHERAL ( 29 FDA reports)
PRIMARY SEQUESTRUM ( 29 FDA reports)
EAR PAIN ( 28 FDA reports)
OSTEONECROSIS OF JAW ( 25 FDA reports)
SPINAL OSTEOARTHRITIS ( 24 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
ABDOMINAL PAIN ( 22 FDA reports)
ASTHENIA ( 22 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
TOOTH EXTRACTION ( 21 FDA reports)
ANAEMIA ( 20 FDA reports)
BACTERIAL INFECTION ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
IMPAIRED HEALING ( 20 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 20 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
ORAL PAIN ( 20 FDA reports)
PLATELET COUNT DECREASED ( 20 FDA reports)
PURULENT DISCHARGE ( 20 FDA reports)
SWELLING ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 19 FDA reports)
ARTHRALGIA ( 19 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 19 FDA reports)
BLOOD GLUCOSE INCREASED ( 19 FDA reports)
BONE DENSITY DECREASED ( 19 FDA reports)
CERVICAL SPINAL STENOSIS ( 19 FDA reports)
COLITIS ( 19 FDA reports)
DEEP VEIN THROMBOSIS ( 19 FDA reports)
DIVERTICULUM INTESTINAL ( 19 FDA reports)
EXOSTOSIS ( 19 FDA reports)
GINGIVAL BLEEDING ( 19 FDA reports)
HAEMATOCHEZIA ( 19 FDA reports)
HEART VALVE INCOMPETENCE ( 19 FDA reports)
HEPATIC CYST ( 19 FDA reports)
INFLAMMATION ( 19 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 19 FDA reports)
LUNG NEOPLASM MALIGNANT ( 19 FDA reports)
NEOPLASM ( 19 FDA reports)
OEDEMA MUCOSAL ( 19 FDA reports)
OSTEOLYSIS ( 19 FDA reports)
OSTEOSCLEROSIS ( 19 FDA reports)
OVARIAN CANCER ( 19 FDA reports)
PERIODONTAL DISEASE ( 19 FDA reports)
RADICULAR PAIN ( 19 FDA reports)
RHINITIS ( 19 FDA reports)
RIB FRACTURE ( 19 FDA reports)
SOFT TISSUE DISORDER ( 19 FDA reports)
STOMATOCYTES PRESENT ( 19 FDA reports)
TENDERNESS ( 19 FDA reports)
ULCER ( 19 FDA reports)
ONYCHOMYCOSIS ( 18 FDA reports)
STOMATITIS ( 18 FDA reports)
ACCIDENT AT WORK ( 17 FDA reports)
BURSITIS ( 17 FDA reports)
EPICONDYLITIS ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
OSTEOARTHRITIS ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
SYNOVIAL CYST ( 17 FDA reports)
SYNOVITIS ( 17 FDA reports)
TENDONITIS ( 17 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
FOREIGN BODY ( 16 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 16 FDA reports)
NECK PAIN ( 16 FDA reports)
RASH MACULO-PAPULAR ( 16 FDA reports)
ONYCHALGIA ( 15 FDA reports)
ARTHROSCOPY ( 14 FDA reports)
LIGAMENT RUPTURE ( 14 FDA reports)
PAIN ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
STRESS FRACTURE ( 14 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CARDIOMEGALY ( 13 FDA reports)
DEBRIDEMENT ( 13 FDA reports)
ENDODONTIC PROCEDURE ( 13 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
JAW OPERATION ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 13 FDA reports)
SLEEP DISORDER ( 13 FDA reports)
SURGERY ( 13 FDA reports)
TENOSYNOVITIS ( 13 FDA reports)
WOUND TREATMENT ( 13 FDA reports)
ANHEDONIA ( 12 FDA reports)
ANXIETY ( 12 FDA reports)
ATROPHY ( 12 FDA reports)
BASAL CELL CARCINOMA ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
DRUG TOXICITY ( 12 FDA reports)
DYSPNOEA ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
GAIT DISTURBANCE ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
OSTEOPENIA ( 12 FDA reports)
OSTEOPOROSIS ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
RADICULOPATHY ( 12 FDA reports)
SCAR ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 11 FDA reports)
CHRONIC SINUSITIS ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
MASS EXCISION ( 11 FDA reports)
MOBILITY DECREASED ( 11 FDA reports)
COUGH ( 10 FDA reports)
GALLBLADDER POLYP ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
STEM CELL TRANSPLANT ( 10 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
RASH ( 9 FDA reports)
SKIN NEOPLASM EXCISION ( 9 FDA reports)
HEADACHE ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
UTERINE PROLAPSE ( 8 FDA reports)
BONE DEBRIDEMENT ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
MELANOCYTIC NAEVUS ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
RASH PRURITIC ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
ARTHRITIS ( 6 FDA reports)
ATELECTASIS ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MULTIPLE FRACTURES ( 6 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LUMBAR SPINAL STENOSIS ( 4 FDA reports)
MALAISE ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
RADICULITIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MYOPERICARDITIS ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVIX CARCINOMA STAGE III ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSE VOLUME DECREASED ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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