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

VOMITING ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
DIARRHOEA ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
DYSPNOEA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
FALL ( 11 FDA reports)
HAEMORRHOIDS ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
INFUSION RELATED REACTION ( 11 FDA reports)
PAIN ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
COMA ( 10 FDA reports)
DISSEMINATED TUBERCULOSIS ( 10 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
LISTERIA ENCEPHALITIS ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
POLYNEUROPATHY ( 10 FDA reports)
XANTHOMA ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
FATIGUE ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
VULVAL ABSCESS ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ASCITES ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
RECTAL FISSURE ( 6 FDA reports)
TREMOR ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
GASTROINTESTINAL INJURY ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
MENINGITIS LISTERIA ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
ENGRAFTMENT SYNDROME ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FEAR ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GERSTMANN'S SYNDROME ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
RALES ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UROGENITAL FISTULA ( 2 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING PSYCHOGENIC ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE ABNORMAL ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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