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

FLUSHING ( 76 FDA reports)
DIZZINESS ( 66 FDA reports)
OEDEMA PERIPHERAL ( 62 FDA reports)
FATIGUE ( 54 FDA reports)
DIARRHOEA ( 52 FDA reports)
PAIN ( 52 FDA reports)
ASTHENIA ( 51 FDA reports)
DYSPNOEA ( 49 FDA reports)
NAUSEA ( 49 FDA reports)
PRURITUS ( 46 FDA reports)
ANXIETY ( 40 FDA reports)
PAIN IN EXTREMITY ( 40 FDA reports)
ARTHRALGIA ( 38 FDA reports)
BACK PAIN ( 36 FDA reports)
WEIGHT DECREASED ( 34 FDA reports)
HYPOTENSION ( 33 FDA reports)
HYPOAESTHESIA ( 32 FDA reports)
PARAESTHESIA ( 32 FDA reports)
INSOMNIA ( 31 FDA reports)
CONSTIPATION ( 29 FDA reports)
INJURY ( 28 FDA reports)
RENAL FAILURE ACUTE ( 28 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 26 FDA reports)
HYPERTENSION ( 25 FDA reports)
PYREXIA ( 25 FDA reports)
ANAEMIA ( 24 FDA reports)
FALL ( 24 FDA reports)
HEADACHE ( 24 FDA reports)
MUSCLE SPASMS ( 24 FDA reports)
SYNCOPE ( 24 FDA reports)
VOMITING ( 24 FDA reports)
WEIGHT INCREASED ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 23 FDA reports)
BLOOD GLUCOSE INCREASED ( 23 FDA reports)
DEHYDRATION ( 23 FDA reports)
MALAISE ( 23 FDA reports)
FEELING HOT ( 22 FDA reports)
PNEUMONIA ( 21 FDA reports)
SOMNOLENCE ( 21 FDA reports)
CEREBROVASCULAR ACCIDENT ( 20 FDA reports)
FEELING ABNORMAL ( 20 FDA reports)
INFECTION ( 20 FDA reports)
PRESYNCOPE ( 20 FDA reports)
TREMOR ( 20 FDA reports)
COUGH ( 19 FDA reports)
ERECTILE DYSFUNCTION ( 19 FDA reports)
LOSS OF CONSCIOUSNESS ( 19 FDA reports)
MUSCULAR WEAKNESS ( 19 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
EMOTIONAL DISTRESS ( 18 FDA reports)
GAIT DISTURBANCE ( 18 FDA reports)
PAIN IN JAW ( 18 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 17 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 17 FDA reports)
ONYCHOMYCOSIS ( 17 FDA reports)
SINUS TACHYCARDIA ( 17 FDA reports)
SINUSITIS ( 17 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
BONE DISORDER ( 16 FDA reports)
BRONCHITIS ( 16 FDA reports)
HYPERLIPIDAEMIA ( 16 FDA reports)
MYALGIA ( 16 FDA reports)
CARDIAC VALVE ABSCESS ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
COLITIS ISCHAEMIC ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DEFORMITY ( 15 FDA reports)
DYSAESTHESIA ( 15 FDA reports)
EPIDIDYMITIS ( 15 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 15 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 15 FDA reports)
HYDROCELE ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
HYPOCALCAEMIA ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
LIBIDO DECREASED ( 15 FDA reports)
LIFE EXPECTANCY SHORTENED ( 15 FDA reports)
MUSCLE TWITCHING ( 15 FDA reports)
NEURALGIA ( 15 FDA reports)
OSTEOMYELITIS ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
PERIPHERAL EMBOLISM ( 15 FDA reports)
PHLEBITIS ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
PROTHROMBIN TIME PROLONGED ( 15 FDA reports)
RENAL ISCHAEMIA ( 15 FDA reports)
SPINAL OSTEOARTHRITIS ( 15 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
TACHYARRHYTHMIA ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
WHEEZING ( 15 FDA reports)
ABDOMINAL DISCOMFORT ( 14 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
DYSPEPSIA ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
CATARACT ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
ERYTHEMA ( 13 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 13 FDA reports)
ORCHITIS ( 13 FDA reports)
RASH ( 13 FDA reports)
TESTICULAR PAIN ( 13 FDA reports)
TESTICULAR SWELLING ( 13 FDA reports)
GYNAECOMASTIA ( 12 FDA reports)
HYPOAESTHESIA FACIAL ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
BURNING SENSATION ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
INJECTION SITE PAIN ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
ALOPECIA ( 10 FDA reports)
CONJUNCTIVITIS ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
CHOLECYSTITIS CHRONIC ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
ATRIAL FLUTTER ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
FEAR ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DIVERTICULITIS ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
OPEN WOUND ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
TENOSYNOVITIS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
ACNE ( 5 FDA reports)
BLINDNESS UNILATERAL ( 5 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
DEATH ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
IRITIS ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HORNER'S SYNDROME ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
STRESS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
ULCER ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYST ( 3 FDA reports)
DEVICE COMPONENT ISSUE ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTRAOCULAR LENS IMPLANT ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLON CANCER STAGE I ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MASS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE ATROPHY ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC CANCER STAGE 0 ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL INFECTION VIRAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL CONSTIPATION ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIBRATORY SENSE INCREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WITHDRAWAL HYPERTENSION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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