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

OSTEONECROSIS OF JAW ( 39 FDA reports)
BONE DISORDER ( 38 FDA reports)
OSTEOTOMY ( 30 FDA reports)
WOUND CLOSURE ( 30 FDA reports)
PAIN ( 21 FDA reports)
DENTAL OPERATION ( 15 FDA reports)
SURGERY ( 13 FDA reports)
DYSPNOEA ( 12 FDA reports)
NAUSEA ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
PRODUCTIVE COUGH ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ATELECTASIS ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
INJURY ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
RESUSCITATION ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
ANHEDONIA ( 8 FDA reports)
ANXIETY ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
BURSITIS ( 8 FDA reports)
CARDIOVASCULAR DISORDER ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
CHEST TUBE INSERTION ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
EDENTULOUS ( 8 FDA reports)
FISTULA DISCHARGE ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPERCHOLESTEROLAEMIA ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MASS ( 8 FDA reports)
METASTASES TO BONE ( 8 FDA reports)
MULTIPLE MYELOMA ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 8 FDA reports)
NECK INJURY ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
PAIN IN JAW ( 8 FDA reports)
PLASMACYTOMA ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 8 FDA reports)
PROTEUS INFECTION ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
RIB FRACTURE ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SPINAL COMPRESSION FRACTURE ( 8 FDA reports)
SPINAL CORPECTOMY ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
SPINAL OSTEOARTHRITIS ( 8 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 8 FDA reports)
TINNITUS ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
ULCER ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABSCESS ORAL ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GINGIVAL PAIN ( 5 FDA reports)
HUNGER ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RETINOBLASTOMA ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
APNOEA ( 3 FDA reports)
BONE OPERATION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
FALL ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
MALAISE ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STENT REMOVAL ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL PIGMENTATION ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)

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