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

ABDOMINAL PAIN ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
OSTEONECROSIS OF JAW ( 7 FDA reports)
PAIN ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
VOMITING ( 7 FDA reports)
CONSTIPATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
EXPOSED BONE IN JAW ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXTERNAL EAR DISORDER ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MACULE ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF CHOROID ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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