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

OSTEONECROSIS ( 34 FDA reports)
DENTAL CARIES ( 26 FDA reports)
ANXIETY ( 24 FDA reports)
DRUG INEFFECTIVE ( 24 FDA reports)
DEPRESSION ( 18 FDA reports)
VARICELLA ( 17 FDA reports)
DYSPHAGIA ( 16 FDA reports)
TOOTH LOSS ( 16 FDA reports)
SINUSITIS ( 15 FDA reports)
ORAL TORUS ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
PAIN ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
ADVERSE EVENT ( 12 FDA reports)
DIZZINESS ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 11 FDA reports)
BONE DISORDER ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
IMPAIRED HEALING ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
MAJOR DEPRESSION ( 10 FDA reports)
ORAL INFECTION ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ABSCESS ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
COUGH ( 8 FDA reports)
EXOSTOSIS ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
OESOPHAGEAL DISCOMFORT ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
TOOTHACHE ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BACK INJURY ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BREAST CANCER METASTATIC ( 7 FDA reports)
BREATH ODOUR ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHILLS ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
FALL ( 7 FDA reports)
FRACTURE ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
LOCAL SWELLING ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
OSTEITIS ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
RHINITIS ALLERGIC ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ADRENAL ADENOMA ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DRUG DEPENDENCE ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HUMAN EHRLICHIOSIS ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BLADDER REPAIR ( 5 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
OOPHORECTOMY ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
STRESS ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
MOUTH INJURY ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
SEBORRHOEIC KERATOSIS ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEGENERATION OF UTERINE FIBROID ( 3 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COMA ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL PRURITUS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERIODONTAL DISEASE ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RASH ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BIOPSY BRAIN ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use