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

CHEST PAIN ( 37 FDA reports)
DIZZINESS ( 35 FDA reports)
NAUSEA ( 35 FDA reports)
DYSPNOEA ( 34 FDA reports)
FATIGUE ( 29 FDA reports)
DRUG INEFFECTIVE ( 26 FDA reports)
HEADACHE ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
DEPRESSION ( 23 FDA reports)
INSOMNIA ( 23 FDA reports)
PAIN ( 22 FDA reports)
MYALGIA ( 20 FDA reports)
ANXIETY ( 19 FDA reports)
HYPERSENSITIVITY ( 19 FDA reports)
PAIN IN EXTREMITY ( 19 FDA reports)
SINUSITIS ( 19 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 18 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
BACK PAIN ( 17 FDA reports)
DIARRHOEA ( 17 FDA reports)
COUGH ( 15 FDA reports)
ASTHMA ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
RASH ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
FALL ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
MUSCLE CRAMP ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
VOMITING ( 12 FDA reports)
BRONCHITIS ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
INJURY ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
TREMOR ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
DYSPEPSIA ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
TROPONIN INCREASED ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PHARYNGITIS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SUICIDAL IDEATION ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
AMNESIA ( 7 FDA reports)
ASCITES ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CHILLS ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
EYE PAIN ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
JAUNDICE ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CHRONIC HEPATITIS ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DIABETIC RETINOPATHY ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
EAR DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
OTITIS EXTERNA ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PIGMENTED NAEVUS ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SLEEP APNOEA SYNDROME ( 6 FDA reports)
SUICIDE ATTEMPT ( 6 FDA reports)
SWEAT DISCOLOURATION ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VENOUS STASIS ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
MANIA ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TRANSFERRIN INCREASED ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPINAL DISORDER ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DESQUAMATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMORAL PULSE ABNORMAL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLINDNESS HYSTERICAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTRON RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
TIC ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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