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

DIARRHOEA ( 47 FDA reports)
NAUSEA ( 41 FDA reports)
PYREXIA ( 41 FDA reports)
ANAEMIA ( 40 FDA reports)
RENAL FAILURE ( 39 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
THROMBOCYTOPENIA ( 31 FDA reports)
PAIN ( 30 FDA reports)
RENAL FAILURE ACUTE ( 30 FDA reports)
VOMITING ( 30 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
DYSPNOEA ( 25 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 22 FDA reports)
FALL ( 22 FDA reports)
PNEUMONIA ( 22 FDA reports)
ASTHENIA ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
CARDIAC ARREST ( 20 FDA reports)
HYPOTENSION ( 19 FDA reports)
MALAISE ( 19 FDA reports)
ABDOMINAL PAIN UPPER ( 18 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 18 FDA reports)
ACUTE PULMONARY OEDEMA ( 17 FDA reports)
CONTUSION ( 17 FDA reports)
LEUKOPENIA ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
BLOOD POTASSIUM DECREASED ( 16 FDA reports)
BURNING SENSATION ( 16 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
HYPERKALAEMIA ( 16 FDA reports)
INFUSION RELATED REACTION ( 16 FDA reports)
PLEURAL EFFUSION ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
ANXIETY ( 15 FDA reports)
BACK PAIN ( 15 FDA reports)
CARDIAC FAILURE ( 15 FDA reports)
CHEST PAIN ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 15 FDA reports)
HOT FLUSH ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 14 FDA reports)
DEATH ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
DEPRESSION ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
BRADYCARDIA ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
DYSKINESIA ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
DYSPEPSIA ( 11 FDA reports)
HAEMATOCRIT DECREASED ( 11 FDA reports)
MALNUTRITION ( 11 FDA reports)
OFF LABEL USE ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
TREMOR ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
DRY MOUTH ( 10 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 9 FDA reports)
INJURY ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PERITONITIS ( 9 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
RENAL TUBULAR NECROSIS ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
ESCHERICHIA SEPSIS ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SUICIDAL IDEATION ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATOCELLULAR INJURY ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANAEMIA NEONATAL ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PNEUMONIA ESCHERICHIA ( 5 FDA reports)
RENAL VESSEL DISORDER ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FOETAL ARRHYTHMIA ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEUTROPENIA NEONATAL ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COLONIC HAEMATOMA ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETROGNATHIA ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APNOEA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PIERRE ROBIN SYNDROME ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THIRST ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONEAL NECROSIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPIGELIAN HERNIA ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TETANY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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