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

DRUG INEFFECTIVE ( 81 FDA reports)
DIARRHOEA ( 68 FDA reports)
VOMITING ( 68 FDA reports)
DYSPNOEA ( 67 FDA reports)
NAUSEA ( 61 FDA reports)
HEADACHE ( 59 FDA reports)
DIZZINESS ( 57 FDA reports)
PYREXIA ( 57 FDA reports)
RASH ( 57 FDA reports)
PNEUMONIA ( 53 FDA reports)
FATIGUE ( 46 FDA reports)
COUGH ( 42 FDA reports)
MALAISE ( 42 FDA reports)
TREMOR ( 42 FDA reports)
ABDOMINAL PAIN ( 41 FDA reports)
ASTHENIA ( 40 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 40 FDA reports)
PRODUCT QUALITY ISSUE ( 39 FDA reports)
DEPRESSION ( 38 FDA reports)
HYPERTENSION ( 36 FDA reports)
BACK PAIN ( 34 FDA reports)
URINARY TRACT INFECTION ( 33 FDA reports)
BRONCHITIS ( 30 FDA reports)
ERYTHEMA ( 30 FDA reports)
FEELING ABNORMAL ( 29 FDA reports)
PAIN ( 28 FDA reports)
CHEST PAIN ( 27 FDA reports)
PLATELET COUNT DECREASED ( 27 FDA reports)
ANXIETY ( 26 FDA reports)
CONFUSIONAL STATE ( 26 FDA reports)
FALL ( 26 FDA reports)
INFECTION ( 25 FDA reports)
NEUROPATHY PERIPHERAL ( 25 FDA reports)
WEIGHT DECREASED ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
CROHN'S DISEASE ( 24 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
OEDEMA PERIPHERAL ( 24 FDA reports)
HAEMORRHAGE ( 23 FDA reports)
INSOMNIA ( 23 FDA reports)
RECTAL HAEMORRHAGE ( 23 FDA reports)
SINUSITIS ( 23 FDA reports)
VISION BLURRED ( 23 FDA reports)
VISUAL DISTURBANCE ( 23 FDA reports)
BLINDNESS ( 22 FDA reports)
DEHYDRATION ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
INTESTINAL HAEMORRHAGE ( 22 FDA reports)
PRURITUS ( 22 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
HYPERSENSITIVITY ( 21 FDA reports)
NEPHROLITHIASIS ( 21 FDA reports)
BLOOD CREATININE INCREASED ( 20 FDA reports)
GASTROINTESTINAL DISORDER ( 20 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
STOMATITIS ( 20 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
JOINT SPRAIN ( 19 FDA reports)
NASOPHARYNGITIS ( 19 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 19 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
NERVE COMPRESSION ( 18 FDA reports)
NIGHT BLINDNESS ( 18 FDA reports)
WHEEZING ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
ABNORMAL BEHAVIOUR ( 17 FDA reports)
AGITATION ( 17 FDA reports)
ANAEMIA ( 17 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
CONSTIPATION ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
LOSS OF CONSCIOUSNESS ( 17 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
NERVOUSNESS ( 17 FDA reports)
PARAESTHESIA ( 17 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
DRUG HYPERSENSITIVITY ( 16 FDA reports)
SOMNOLENCE ( 16 FDA reports)
COLITIS ULCERATIVE ( 15 FDA reports)
DYSPHAGIA ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
RENAL FAILURE ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
AGGRESSION ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 14 FDA reports)
HYPOAESTHESIA ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
SUICIDAL IDEATION ( 14 FDA reports)
ASTHMA ( 13 FDA reports)
CARPAL TUNNEL SYNDROME ( 13 FDA reports)
CHILLS ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
DYSGEUSIA ( 13 FDA reports)
DYSPEPSIA ( 13 FDA reports)
FLUSHING ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
DEATH ( 12 FDA reports)
EATING DISORDER ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
ILL-DEFINED DISORDER ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
RHINORRHOEA ( 12 FDA reports)
ATRIAL SEPTAL DEFECT ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CLOSTRIDIAL INFECTION ( 11 FDA reports)
HALLUCINATION ( 11 FDA reports)
MENTAL DISORDER ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
TACHYPNOEA ( 11 FDA reports)
ABDOMINAL DISCOMFORT ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 10 FDA reports)
CATARACT ( 10 FDA reports)
COMA ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
IRRITABILITY ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
NEUTROPHIL COUNT DECREASED ( 10 FDA reports)
OROPHARYNGEAL PAIN ( 10 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
SWELLING FACE ( 10 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
BLOOD CALCIUM DECREASED ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
BRONCHOSPASM ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
FUNGAL INFECTION ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
SUICIDE ATTEMPT ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
TUMOUR LYSIS SYNDROME ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
ANOSMIA ( 8 FDA reports)
APHASIA ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 8 FDA reports)
CRYING ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
OLIGURIA ( 8 FDA reports)
STOMACH DISCOMFORT ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
ABASIA ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 7 FDA reports)
AGEUSIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
BRONCHIOLITIS ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
FEELING HOT ( 7 FDA reports)
FLANK PAIN ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
MUSCULOSKELETAL DISORDER ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
NECK INJURY ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
ORAL FUNGAL INFECTION ( 7 FDA reports)
PAROSMIA ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PULMONARY VALVE STENOSIS ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SWELLING ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CHOKING ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 6 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
DYSMORPHISM ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
ENTEROBACTER BACTERAEMIA ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FEAR ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
FOLLICULITIS ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INJECTION SITE PAIN ( 6 FDA reports)
INJURY ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NOONAN SYNDROME ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PULMONARY ARTERY DILATATION ( 6 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STRABISMUS ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ANAL ABSCESS ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
BACK INJURY ( 5 FDA reports)
BIPOLAR DISORDER ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CYST ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
DEVELOPMENTAL DELAY ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
MANIA ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SUPERFICIAL INJURY OF EYE ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
VULVAL OEDEMA ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACNE ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CRYPTORCHISM ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EAGLE BARRETT SYNDROME ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
EXPIRED DRUG ADMINISTERED ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
KIDNEY MALFORMATION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
METASTATIC NEOPLASM ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
REBOUND HYPERTENSION ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RHINITIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TALIPES ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TIC ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
UNINTENDED PREGNANCY ( 4 FDA reports)
VAGINAL ABSCESS ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
CONGENITAL AORTIC STENOSIS ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEOSTOMY CLOSURE ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LOWER LIMB FRACTURE ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RETCHING ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCAR ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VAGINAL SWELLING ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
AUTISM ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DESQUAMATION MOUTH ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POISONING ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
ULCER ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URINE CHLORIDE DECREASED ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNIOCENTESIS ABNORMAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGENITAL HEPATOMEGALY ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS FUNGAL ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FACE LIFT ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JEJUNAL STENOSIS ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE INFECTION ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL EXUDATE ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRENATAL SCREENING TEST ABNORMAL ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THELITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBAL RUPTURE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULTRASOUND SKULL ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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