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

FATIGUE ( 89 FDA reports)
APPLICATION SITE ERYTHEMA ( 77 FDA reports)
INFLUENZA LIKE ILLNESS ( 76 FDA reports)
HEADACHE ( 60 FDA reports)
PYREXIA ( 58 FDA reports)
DIZZINESS ( 56 FDA reports)
NAUSEA ( 56 FDA reports)
MYALGIA ( 52 FDA reports)
PAIN ( 48 FDA reports)
APPLICATION SITE REACTION ( 46 FDA reports)
RASH ( 44 FDA reports)
ASTHENIA ( 43 FDA reports)
LYMPHADENOPATHY ( 43 FDA reports)
ARTHRALGIA ( 40 FDA reports)
APPLICATION SITE PAIN ( 37 FDA reports)
DYSPNOEA ( 37 FDA reports)
ECZEMA ( 37 FDA reports)
ERYTHEMA ( 36 FDA reports)
MALAISE ( 33 FDA reports)
CONDITION AGGRAVATED ( 31 FDA reports)
APPLICATION SITE IRRITATION ( 30 FDA reports)
EAR INFECTION ( 30 FDA reports)
DEPRESSION ( 29 FDA reports)
PNEUMONIA ( 29 FDA reports)
SCAB ( 29 FDA reports)
WEIGHT DECREASED ( 29 FDA reports)
ANXIETY ( 28 FDA reports)
BACK PAIN ( 28 FDA reports)
CHEST PAIN ( 28 FDA reports)
APPLICATION SITE OEDEMA ( 27 FDA reports)
RHINITIS ALLERGIC ( 27 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
URTICARIA ( 25 FDA reports)
SKIN LESION ( 24 FDA reports)
DIARRHOEA ( 23 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 23 FDA reports)
APPLICATION SITE SCAB ( 22 FDA reports)
APPLICATION SITE INFLAMMATION ( 21 FDA reports)
CHILLS ( 21 FDA reports)
ALOPECIA ( 20 FDA reports)
APPLICATION SITE ULCER ( 20 FDA reports)
HYPOAESTHESIA ( 20 FDA reports)
NIGHT SWEATS ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
VOMITING ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
APPLICATION SITE PRURITUS ( 19 FDA reports)
KELOID SCAR ( 19 FDA reports)
PAIN IN EXTREMITY ( 19 FDA reports)
COUGH ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
PALPITATIONS ( 18 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
CHEST DISCOMFORT ( 17 FDA reports)
FALL ( 17 FDA reports)
GINGIVAL RECESSION ( 17 FDA reports)
HODGKIN'S DISEASE ( 17 FDA reports)
JOINT SWELLING ( 17 FDA reports)
LARYNGOCELE ( 17 FDA reports)
PNEUMOTHORAX ( 17 FDA reports)
THROMBOSIS ( 17 FDA reports)
CYST ( 16 FDA reports)
DYSPAREUNIA ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
INFLAMMATION ( 16 FDA reports)
PYELOCALIECTASIS ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
VAGINAL HAEMORRHAGE ( 16 FDA reports)
APPLICATION SITE DESQUAMATION ( 15 FDA reports)
APPLICATION SITE DISCHARGE ( 15 FDA reports)
BASAL CELL CARCINOMA ( 15 FDA reports)
BLADDER DILATATION ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
DYSURIA ( 15 FDA reports)
ERYTHEMA MULTIFORME ( 14 FDA reports)
HAND FRACTURE ( 14 FDA reports)
HEAD INJURY ( 14 FDA reports)
RASH MACULAR ( 14 FDA reports)
REFLUX LARYNGITIS ( 14 FDA reports)
SUICIDAL IDEATION ( 14 FDA reports)
CONJUNCTIVITIS ( 13 FDA reports)
LUNG DISORDER ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
PYODERMA GANGRENOSUM ( 13 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
DERMATOMYOSITIS ( 12 FDA reports)
DYSPHONIA ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
TREMOR ( 12 FDA reports)
VISION BLURRED ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
SWELLING ( 11 FDA reports)
THIRST ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ALLERGY TO ANIMAL ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BURNING SENSATION ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CHRONIC SINUSITIS ( 10 FDA reports)
DERMATITIS ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DYSPEPSIA ( 10 FDA reports)
ECZEMA EYELIDS ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
REFLUX OESOPHAGITIS ( 10 FDA reports)
SKIN DISCOLOURATION ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
ANOREXIA ( 9 FDA reports)
APPLICATION SITE DISCOLOURATION ( 9 FDA reports)
APPLICATION SITE INFECTION ( 9 FDA reports)
APPLICATION SITE SWELLING ( 9 FDA reports)
APPLICATION SITE VESICLES ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BLISTER ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
MENTAL DISORDER ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
VIRAL PHARYNGITIS ( 9 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BIOPSY LYMPH GLAND ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 8 FDA reports)
EXCORIATION ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HEPATIC CYST ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
LUNG NEOPLASM ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
MASS ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SKIN REACTION ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
TINNITUS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
AGITATION ( 7 FDA reports)
ANGER ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
APPLICATION SITE EXFOLIATION ( 7 FDA reports)
BIPOLAR DISORDER ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DECREASED INTEREST ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
EAR PAIN ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
GROIN PAIN ( 7 FDA reports)
HAEMORRHOIDS ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANIMAL BITE ( 6 FDA reports)
APPLICATION SITE BLEEDING ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
BONE LESION ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
DEATH ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INFECTION ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
LIP PAIN ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MULTIPLE MYELOMA ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NECROSIS ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
PELVIC FRACTURE ( 6 FDA reports)
PLASMACYTOMA ( 6 FDA reports)
PSORIASIS ( 6 FDA reports)
PULMONARY MASS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SCAR ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
TOOTHACHE ( 6 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ACNE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
APNOEA ( 5 FDA reports)
APPLICATION SITE DRYNESS ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BRONCHOMALACIA ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEAFNESS UNILATERAL ( 5 FDA reports)
DERMAL CYST ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
EXOMPHALOS ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LARYNGOMALACIA ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
OPEN WOUND ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TRACHEOMALACIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
APPLICATION SITE EROSION ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MAMMOGRAM ABNORMAL ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
PRECANCEROUS SKIN LESION ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
ULCER ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
WOUND SECRETION ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ASPIRATION BREAST ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BREAST INFECTION ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CRYING ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
FACIAL LESION EXCISION ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
GINGIVAL ULCERATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTROPHIC SCAR ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
IRITIS ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ONYCHALGIA ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
TOURETTE'S DISORDER ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE NECROSIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD GLUCAGON INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BUNION ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL PAIN FEMALE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LENTIGO ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOCALISED SKIN REACTION ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NAIL PSORIASIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POISONING ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TESTIS DISCOMFORT ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE ABSCESS ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BOWENOID PAPULOSIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRIS EXFOLIATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOSALPINGITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHERESIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELOCYSTITIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYMUS ENLARGEMENT ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CERVIX HYPERTROPHY ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
VAGINAL CELLULITIS ( 1 FDA reports)
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VAGINAL LACERATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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