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FATIGUE ( 24 FDA reports)
DIZZINESS ( 22 FDA reports)
MALAISE ( 22 FDA reports)
NAUSEA ( 20 FDA reports)
CHOLELITHIASIS ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
DYSPNOEA ( 17 FDA reports)
CHEST PAIN ( 16 FDA reports)
INSOMNIA ( 16 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
BACK PAIN ( 13 FDA reports)
BLOOD PRESSURE INCREASED ( 13 FDA reports)
GASTROINTESTINAL INFECTION ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
NAIL INFECTION ( 13 FDA reports)
VOMITING ( 13 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
PYREXIA ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
FALL ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
COUGH ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
TREMOR ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PAIN ( 6 FDA reports)
RASH ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
INJURY ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NODULE ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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