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

BREAST CANCER ( 456 FDA reports)
BREAST CANCER FEMALE ( 231 FDA reports)
BREAST CANCER METASTATIC ( 80 FDA reports)
PAIN ( 72 FDA reports)
ANXIETY ( 68 FDA reports)
NAUSEA ( 43 FDA reports)
DEPRESSION ( 39 FDA reports)
HEADACHE ( 35 FDA reports)
OSTEONECROSIS OF JAW ( 34 FDA reports)
DIZZINESS ( 33 FDA reports)
FALL ( 33 FDA reports)
BREAST CANCER IN SITU ( 30 FDA reports)
LOOSE TOOTH ( 29 FDA reports)
TOOTH DISORDER ( 29 FDA reports)
OSTEOPOROSIS ( 28 FDA reports)
SENSITIVITY OF TEETH ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
BACK PAIN ( 27 FDA reports)
BONE DISORDER ( 27 FDA reports)
INJURY ( 26 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 25 FDA reports)
OSTEOMYELITIS ( 25 FDA reports)
PYREXIA ( 25 FDA reports)
DIARRHOEA ( 24 FDA reports)
FATIGUE ( 23 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
IMPAIRED HEALING ( 22 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
VISION BLURRED ( 22 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
FEMUR FRACTURE ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
DIPLOPIA ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
DRY MOUTH ( 18 FDA reports)
GAIT DISTURBANCE ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
HOT FLUSH ( 18 FDA reports)
HYPOAESTHESIA ( 18 FDA reports)
INSOMNIA ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
ASTHENIA ( 17 FDA reports)
DYSPNOEA ( 17 FDA reports)
FISTULA ( 17 FDA reports)
INFECTION ( 17 FDA reports)
OSTEORADIONECROSIS ( 17 FDA reports)
SCAR ( 17 FDA reports)
TOOTH LOSS ( 17 FDA reports)
VISUAL ACUITY REDUCED ( 17 FDA reports)
VOMITING ( 17 FDA reports)
DYSGEUSIA ( 16 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
TOOTH FRACTURE ( 16 FDA reports)
ANHEDONIA ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
CONSTIPATION ( 15 FDA reports)
CONVULSION ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DEFORMITY ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
LIP SWELLING ( 15 FDA reports)
OSTEOARTHRITIS ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
PHOTOPSIA ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
SKIN PAPILLOMA ( 15 FDA reports)
TOOTH EXTRACTION ( 15 FDA reports)
VISUAL IMPAIRMENT ( 15 FDA reports)
VITREOUS FLOATERS ( 15 FDA reports)
COUGH ( 14 FDA reports)
EATING DISORDER ( 14 FDA reports)
GINGIVAL BLEEDING ( 14 FDA reports)
MOUTH HAEMORRHAGE ( 14 FDA reports)
ORAL CAVITY FISTULA ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PULMONARY HYPERTENSION ( 14 FDA reports)
SECONDARY SEQUESTRUM ( 14 FDA reports)
AMNESIA ( 13 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 13 FDA reports)
BODY TEMPERATURE INCREASED ( 13 FDA reports)
CANDIDIASIS ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
DENTAL CARIES ( 13 FDA reports)
FEELING ABNORMAL ( 13 FDA reports)
METASTASES TO BONE ( 13 FDA reports)
NEOPLASM ( 13 FDA reports)
PAIN IN JAW ( 13 FDA reports)
TOOTH INFECTION ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
BLOOD PRESSURE ABNORMAL ( 12 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
DENTAL PROSTHESIS USER ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
EDENTULOUS ( 12 FDA reports)
EMPHYSEMA ( 12 FDA reports)
GINGIVAL PAIN ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
MALAISE ( 12 FDA reports)
MALNUTRITION ( 12 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 12 FDA reports)
NEOPLASM RECURRENCE ( 12 FDA reports)
OESOPHAGITIS ( 12 FDA reports)
PERIODONTITIS ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
PNEUMONITIS ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
RIB FRACTURE ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ABDOMINAL DISCOMFORT ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
FOOT DEFORMITY ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
HYPERKERATOSIS ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
HYPERTONIC BLADDER ( 11 FDA reports)
MULTIPLE MYELOMA ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
ONYCHOMYCOSIS ( 11 FDA reports)
ORAL DISORDER ( 11 FDA reports)
OSTEOPENIA ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
PAROSMIA ( 11 FDA reports)
RHINITIS ALLERGIC ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
ARTHRITIS ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
MARITAL PROBLEM ( 10 FDA reports)
MASTECTOMY ( 10 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 10 FDA reports)
ALOPECIA ( 9 FDA reports)
BENIGN BREAST NEOPLASM ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BREAST DISORDER ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HEAD INJURY ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
BACK DISORDER ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DENTAL IMPLANTATION ( 8 FDA reports)
EAR CONGESTION ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
RADIATION SKIN INJURY ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ABNORMAL DREAMS ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
MALIGNANT TUMOUR EXCISION ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
RADIOTHERAPY ( 7 FDA reports)
RADIOTHERAPY TO BRAIN ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
STRESS ( 7 FDA reports)
THORACOTOMY ( 7 FDA reports)
ULCER ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
ATELECTASIS ( 6 FDA reports)
BREAST MASS ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
DYSPLASIA ( 6 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
MENISCUS LESION ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
RASH ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SURGERY ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BREAST CANCER STAGE II ( 5 FDA reports)
BREAST INFECTION ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CERVICOBRACHIAL SYNDROME ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DEATH ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
HYPOPHOSPHATASIA ( 5 FDA reports)
IMPLANT SITE SWELLING ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MONOCLONAL GAMMOPATHY ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PARAPROTEINAEMIA ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
CRANIECTOMY ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
OSTEOLYSIS ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POST PROCEDURAL CELLULITIS ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINAL CYST ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
APATHY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE LOSS ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYST ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
FEAR ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 2 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT LABEL CONFUSION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PACKAGING ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
VAGINAL STRICTURE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VULVOVAGINAL ADHESION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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