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

ANXIETY ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PAIN ( 9 FDA reports)
DRY EYE ( 7 FDA reports)
FALL ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
ANKLE FRACTURE ( 6 FDA reports)
BONE DEBRIDEMENT ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
ORAL SURGERY ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
ROTATOR CUFF REPAIR ( 6 FDA reports)
ROTATOR CUFF SYNDROME ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
JOINT DISLOCATION REDUCTION ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
ULNAR NEURITIS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONJUNCTIVOCHALASIS ( 3 FDA reports)
CORNEAL DYSTROPHY ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
GLARE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERTRIGO ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PHYSICAL DISABILITY ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
SCAR ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STARING ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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