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

NAUSEA ( 59 FDA reports)
PAIN ( 40 FDA reports)
CHOLELITHIASIS ( 34 FDA reports)
DIARRHOEA ( 33 FDA reports)
DEEP VEIN THROMBOSIS ( 31 FDA reports)
CHEST PAIN ( 30 FDA reports)
CHOLECYSTITIS CHRONIC ( 30 FDA reports)
BACK PAIN ( 29 FDA reports)
FATIGUE ( 29 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
ARTHRALGIA ( 25 FDA reports)
VOMITING ( 25 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
ANXIETY ( 23 FDA reports)
ASTHENIA ( 23 FDA reports)
INJURY ( 22 FDA reports)
HYPERTENSION ( 21 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
DEPRESSION ( 20 FDA reports)
PULMONARY EMBOLISM ( 20 FDA reports)
GAIT DISTURBANCE ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
MALAISE ( 19 FDA reports)
RASH ( 19 FDA reports)
WEIGHT INCREASED ( 19 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 18 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
DIZZINESS ( 18 FDA reports)
HYPOKALAEMIA ( 18 FDA reports)
DYSPNOEA ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 16 FDA reports)
PLEURAL EFFUSION ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
DIABETES MELLITUS ( 15 FDA reports)
ERYTHEMA ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
FALL ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
SPINAL OSTEOARTHRITIS ( 14 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
MALNUTRITION ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
HERPES ZOSTER ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 12 FDA reports)
JOINT EFFUSION ( 12 FDA reports)
LEUKOCYTOSIS ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
CHOLECYSTITIS ACUTE ( 11 FDA reports)
CHRONIC SINUSITIS ( 11 FDA reports)
LUNG DISORDER ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
OSTEONECROSIS ( 11 FDA reports)
OSTEONECROSIS OF JAW ( 11 FDA reports)
OSTEOPENIA ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RENAL TUBULAR ACIDOSIS ( 11 FDA reports)
RIB FRACTURE ( 11 FDA reports)
ADRENAL INSUFFICIENCY ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DUODENAL POLYP ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
LUNG NEOPLASM ( 10 FDA reports)
METASTASES TO BONE ( 10 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 10 FDA reports)
OSTEOSCLEROSIS ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PROTHROMBIN TIME PROLONGED ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SPINAL COMPRESSION FRACTURE ( 10 FDA reports)
SPINAL FRACTURE ( 10 FDA reports)
SPONDYLOLISTHESIS ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
CHILLS ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
LUNG INFILTRATION ( 9 FDA reports)
OBESITY ( 9 FDA reports)
PANCREATITIS ( 9 FDA reports)
PROTEINURIA ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
TARDIVE DYSKINESIA ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
SCAR ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
COMA ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
LIPOMA ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ABSCESS ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
DEATH ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
FEAR ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GALLBLADDER INJURY ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PRESYNCOPE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BREAST MASS ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
FISTULA ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
FUNGAL SEPSIS ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HEPATIC STEATOSIS ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
JAW OPERATION ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
LOBAR PNEUMONIA ( 5 FDA reports)
MAXILLOFACIAL OPERATION ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
SHORT-BOWEL SYNDROME ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
STRESS ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BIOPSY BREAST ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MAMMOGRAM ABNORMAL ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
TREMOR ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
TYPE 1 DIABETES MELLITUS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POISONING ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BREAST RECONSTRUCTION ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOREA ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
AURA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
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MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
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OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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