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BREAST CANCER FEMALE ( 213 FDA reports)
BREAST CANCER ( 112 FDA reports)
ANXIETY ( 45 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 32 FDA reports)
PAIN ( 28 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 25 FDA reports)
DEPRESSION ( 21 FDA reports)
INJURY ( 21 FDA reports)
FATIGUE ( 18 FDA reports)
METRORRHAGIA ( 17 FDA reports)
DEEP VEIN THROMBOSIS ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
CHEST PAIN ( 15 FDA reports)
HEADACHE ( 15 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
COUGH ( 13 FDA reports)
DYSPNOEA ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
BREAST CANCER IN SITU ( 12 FDA reports)
MASTECTOMY ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
BREAST MASS ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
MENORRHAGIA ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
VOMITING ( 9 FDA reports)
CELLULITIS ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
MARITAL PROBLEM ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
UTERINE LEIOMYOMA ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BREAST CANCER METASTATIC ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SMEAR CERVIX ABNORMAL ( 7 FDA reports)
TREMOR ( 7 FDA reports)
VAGINAL DISCHARGE ( 7 FDA reports)
ALOPECIA ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BONE DENSITY DECREASED ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREAST RECONSTRUCTION ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
FALLOPIAN TUBE DISORDER ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC POLYPS ( 5 FDA reports)
GENITAL DISORDER FEMALE ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
INFECTION ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
LABILE HYPERTENSION ( 5 FDA reports)
LACTOSE INTOLERANCE ( 5 FDA reports)
LOSS OF LIBIDO ( 5 FDA reports)
LYMPHOEDEMA ( 5 FDA reports)
MACROGNATHIA ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MENISCUS LESION ( 5 FDA reports)
MENISCUS OPERATION ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
VAGINAL DISORDER ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC LESION ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SCAN LYMPH NODES ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ENDOMETRIAL ABLATION ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
IUD MIGRATION ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEURILEMMOMA ( 3 FDA reports)
NEURODERMATITIS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETINOPATHY PROLIFERATIVE ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SOFT TISSUE DISORDER ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONTRALATERAL BREAST CANCER ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEAR ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MANIA ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PITYRIASIS RUBRA PILARIS ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVULATION INDUCTION ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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