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

PAIN ( 96 FDA reports)
DYSPNOEA ( 80 FDA reports)
ANXIETY ( 63 FDA reports)
NAUSEA ( 59 FDA reports)
FATIGUE ( 58 FDA reports)
VOMITING ( 53 FDA reports)
INJURY ( 50 FDA reports)
CHOLELITHIASIS ( 49 FDA reports)
ABDOMINAL PAIN ( 47 FDA reports)
HYPOAESTHESIA ( 47 FDA reports)
DEPRESSION ( 46 FDA reports)
DIZZINESS ( 46 FDA reports)
HEADACHE ( 45 FDA reports)
FALL ( 40 FDA reports)
WEIGHT DECREASED ( 40 FDA reports)
ASTHENIA ( 39 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 39 FDA reports)
PULMONARY EMBOLISM ( 38 FDA reports)
DEEP VEIN THROMBOSIS ( 36 FDA reports)
DIARRHOEA ( 36 FDA reports)
INSOMNIA ( 35 FDA reports)
CHEST DISCOMFORT ( 34 FDA reports)
ARTHRALGIA ( 33 FDA reports)
CHOLECYSTITIS CHRONIC ( 33 FDA reports)
FEMUR FRACTURE ( 33 FDA reports)
MALAISE ( 33 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
CHEST PAIN ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
BACK PAIN ( 29 FDA reports)
DRUG INEFFECTIVE ( 29 FDA reports)
PALPITATIONS ( 29 FDA reports)
PARAESTHESIA ( 29 FDA reports)
GALLBLADDER DISORDER ( 27 FDA reports)
MUSCLE SPASMS ( 27 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
EMOTIONAL DISTRESS ( 25 FDA reports)
LOW TURNOVER OSTEOPATHY ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
CONSTIPATION ( 24 FDA reports)
FEELING ABNORMAL ( 24 FDA reports)
MEDICATION RESIDUE ( 24 FDA reports)
SINUSITIS ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 23 FDA reports)
JAUNDICE ( 23 FDA reports)
PNEUMONIA ( 23 FDA reports)
CONVULSION ( 22 FDA reports)
DRUG HYPERSENSITIVITY ( 22 FDA reports)
PRURITUS ( 22 FDA reports)
URINARY INCONTINENCE ( 22 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
BONE DISORDER ( 21 FDA reports)
OSTEOARTHRITIS ( 21 FDA reports)
VERTIGO ( 21 FDA reports)
COUGH ( 20 FDA reports)
FRACTURE NONUNION ( 20 FDA reports)
HEPATIC ENZYME INCREASED ( 20 FDA reports)
LARYNGITIS ( 20 FDA reports)
MYOCARDIAL INFARCTION ( 20 FDA reports)
SPINAL OSTEOARTHRITIS ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
DYSPEPSIA ( 19 FDA reports)
DYSPHAGIA ( 19 FDA reports)
ASTHMA ( 18 FDA reports)
CHILLS ( 18 FDA reports)
OSTEOPOROSIS ( 18 FDA reports)
PAIN IN EXTREMITY ( 18 FDA reports)
TREMOR ( 18 FDA reports)
ABDOMINAL DISCOMFORT ( 17 FDA reports)
ANOREXIA ( 17 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
HYPERTENSION ( 17 FDA reports)
KNEE ARTHROPLASTY ( 17 FDA reports)
MASS ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
THYROID DISORDER ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
CORONARY ARTERY DISEASE ( 16 FDA reports)
INFECTION ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
ADVERSE EVENT ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
CYSTITIS INTERSTITIAL ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
MACULAR DEGENERATION ( 15 FDA reports)
NECK PAIN ( 15 FDA reports)
SINUS DISORDER ( 15 FDA reports)
ABDOMINAL DISTENSION ( 14 FDA reports)
ANHEDONIA ( 14 FDA reports)
ARTHROPATHY ( 14 FDA reports)
CHROMATURIA ( 14 FDA reports)
DRY MOUTH ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
NEUROPATHY PERIPHERAL ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
LOWER LIMB FRACTURE ( 13 FDA reports)
TIBIA FRACTURE ( 13 FDA reports)
WHEEZING ( 13 FDA reports)
AGITATION ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
FEMORAL NECK FRACTURE ( 12 FDA reports)
SINUS CONGESTION ( 12 FDA reports)
ATELECTASIS ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
BRONCHOSPASM ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
CHOLECYSTITIS ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
ARTHRITIS ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
CARPAL TUNNEL SYNDROME ( 10 FDA reports)
DEFORMITY ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DEVICE FAILURE ( 10 FDA reports)
EROSIVE OESOPHAGITIS ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
MENTAL DISORDER ( 10 FDA reports)
NASAL SEPTUM DEVIATION ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NERVOUS SYSTEM DISORDER ( 10 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TENDONITIS ( 10 FDA reports)
THIRST ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
HERPES SIMPLEX ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
INJECTION SITE PAIN ( 9 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
OSTEONECROSIS OF JAW ( 9 FDA reports)
PANIC ATTACK ( 9 FDA reports)
RADIUS FRACTURE ( 9 FDA reports)
RASH ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
REFLUX LARYNGITIS ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
SKIN DISORDER ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
DERMATOMYOSITIS ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
HYPOTHYROIDISM ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
ORAL CANDIDIASIS ( 8 FDA reports)
POLLAKIURIA ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
ROAD TRAFFIC ACCIDENT ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
SPINAL COLUMN STENOSIS ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TOOTH INFECTION ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
FOREARM FRACTURE ( 7 FDA reports)
GALLBLADDER OEDEMA ( 7 FDA reports)
GANGRENE ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATIC CYST ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
LOCALISED INFECTION ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
METASTASES TO LYMPH NODES ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
OBESITY ( 7 FDA reports)
OESOPHAGEAL SPASM ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
SCAB ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ANGER ( 6 FDA reports)
APATHY ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BIOPSY BREAST ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
CERVICAL DYSPLASIA ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CRYING ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
FEAR ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HEMIPLEGIA ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
KIDNEY INFECTION ( 6 FDA reports)
LABORATORY TEST ABNORMAL ( 6 FDA reports)
LUNG NEOPLASM ( 6 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
PATHOLOGICAL FRACTURE ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PRIMARY SEQUESTRUM ( 6 FDA reports)
RECTOCELE ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SMEAR CERVIX ABNORMAL ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
URETHRAL CARUNCLE ( 6 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CLUSTER HEADACHE ( 5 FDA reports)
COMA ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DENTAL PLAQUE ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 5 FDA reports)
EXPOSED BONE IN JAW ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FRACTURE DISPLACEMENT ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTENTION TREMOR ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LOBAR PNEUMONIA ( 5 FDA reports)
MACROCYTOSIS ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
ORAL CAVITY FISTULA ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
SPINAL CORD DISORDER ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TERATOMA ( 5 FDA reports)
THYROIDITIS CHRONIC ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
BACK DISORDER ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ESSENTIAL TREMOR ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MICTURITION URGENCY ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
SCAR ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
STRESS ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
THALAMUS HAEMORRHAGE ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VASOMOTOR RHINITIS ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
VITAMIN D DEFICIENCY ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ALLERGY TO VACCINE ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEPATIC LESION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PURPURA SENILE ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SNORING ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIP DEFORMITY ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MAMMARY DUCT ECTASIA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL POLYP ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AURA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERENNIAL ALLERGY ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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