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

ANAEMIA ( 33 FDA reports)
METASTASES TO BONE ( 30 FDA reports)
DYSPNOEA ( 27 FDA reports)
OSTEONECROSIS OF JAW ( 27 FDA reports)
BREAST CANCER METASTATIC ( 24 FDA reports)
ANXIETY ( 23 FDA reports)
COMPRESSION FRACTURE ( 23 FDA reports)
DISABILITY ( 23 FDA reports)
PAIN ( 23 FDA reports)
MUSCULOSKELETAL PAIN ( 22 FDA reports)
NAUSEA ( 22 FDA reports)
BACK PAIN ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
METASTASES TO LIVER ( 19 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 18 FDA reports)
DIARRHOEA ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
MYOSITIS ( 17 FDA reports)
OSTEOARTHRITIS ( 17 FDA reports)
PLEURAL EFFUSION ( 17 FDA reports)
VOMITING ( 16 FDA reports)
PNEUMONIA ( 15 FDA reports)
BONE DISORDER ( 14 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 14 FDA reports)
SPINAL OSTEOARTHRITIS ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
BONE LESION ( 13 FDA reports)
NEUTROPENIA ( 13 FDA reports)
PRODUCTIVE COUGH ( 13 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 12 FDA reports)
ANHEDONIA ( 12 FDA reports)
AXILLARY MASS ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
BRACHIAL PLEXOPATHY ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
DEAFNESS ( 12 FDA reports)
DENTAL CARIES ( 12 FDA reports)
DENTURE WEARER ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
EMPHYSEMA ( 12 FDA reports)
GASTRITIS ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
IMPAIRED HEALING ( 12 FDA reports)
INJURY ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
MALAISE ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
NECK PAIN ( 12 FDA reports)
OESOPHAGEAL ULCER ( 12 FDA reports)
OESOPHAGITIS ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
SENSITIVITY OF TEETH ( 12 FDA reports)
TOOTH ABSCESS ( 12 FDA reports)
TOOTHACHE ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
BONE PAIN ( 11 FDA reports)
DECREASED INTEREST ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
FALL ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
HIP FRACTURE ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
PERICARDIAL EFFUSION ( 11 FDA reports)
WEIGHT BEARING DIFFICULTY ( 11 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
JOINT EFFUSION ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
SPINAL COMPRESSION FRACTURE ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
LUNG INFILTRATION ( 9 FDA reports)
NASAL CONGESTION ( 9 FDA reports)
RENAL CYST ( 9 FDA reports)
SINUSITIS ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ASCITES ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 8 FDA reports)
CLOSED FRACTURE MANIPULATION ( 8 FDA reports)
EAR PAIN ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
PLEURITIC PAIN ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
RADIOTHERAPY ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
TRANSFUSION ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
ENTEROCOCCAL INFECTION ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
FEMUR FRACTURE ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PELVIC PAIN ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
UTERINE ATONY ( 7 FDA reports)
UTERINE PROLAPSE ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BONE DEBRIDEMENT ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
NERVE BLOCK ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
OVARIAN ADHESION ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
RASH ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
FASCIITIS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
COLPORRHAPHY ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
ENDODONTIC PROCEDURE ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
OSTEOLYSIS ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TREMOR ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VAGINOPLASTY ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
ACNE ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANIMAL BITE ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
DEATH ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
LIP DRY ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SWELLING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MESENTERIC ATHEROSCLEROSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
STUPOR ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)

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