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

BONE DISORDER ( 23 FDA reports)
OSTEONECROSIS OF JAW ( 21 FDA reports)
OSTEOTOMY ( 20 FDA reports)
PAIN ( 20 FDA reports)
WOUND CLOSURE ( 20 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
NAUSEA ( 13 FDA reports)
HEADACHE ( 11 FDA reports)
ASTHENIA ( 9 FDA reports)
DENTAL OPERATION ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SURGERY ( 8 FDA reports)
VOMITING ( 8 FDA reports)
ANAESTHETIC COMPLICATION ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CATARACT ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
TOOTH EXTRACTION ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DIPLEGIA ( 5 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ARACHNOIDITIS ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
GRAFT HAEMORRHAGE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUTISM ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
WOUND DRAINAGE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TETANY ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANAESTHETIC COMPLICATION VASCULAR ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL RUBELLA INFECTION ( 1 FDA reports)
CONGENITAL VARICELLA INFECTION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECTOPIC KIDNEY ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FALLOPIAN TUBE OPERATION ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOETAL METHOTREXATE SYNDROME ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TALIPES ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VULVOVAGINAL ADHESION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use