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

PYREXIA ( 83 FDA reports)
ABDOMINAL PAIN ( 80 FDA reports)
DRUG INTERACTION ( 64 FDA reports)
ASTHENIA ( 57 FDA reports)
DYSPNOEA ( 52 FDA reports)
PAIN ( 52 FDA reports)
MALAISE ( 51 FDA reports)
DEEP VEIN THROMBOSIS ( 50 FDA reports)
NAUSEA ( 49 FDA reports)
HAEMOGLOBIN DECREASED ( 45 FDA reports)
RETROPERITONEAL HAEMATOMA ( 45 FDA reports)
HYPOVOLAEMIC SHOCK ( 44 FDA reports)
VOMITING ( 44 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 42 FDA reports)
HYPOTENSION ( 41 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 41 FDA reports)
RENAL FAILURE ( 39 FDA reports)
DIZZINESS ( 38 FDA reports)
URETERIC OBSTRUCTION ( 38 FDA reports)
MYOCARDIAL INFARCTION ( 37 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
FALL ( 36 FDA reports)
FATIGUE ( 36 FDA reports)
DIARRHOEA ( 35 FDA reports)
MUSCLE HAEMORRHAGE ( 34 FDA reports)
CHEST PAIN ( 33 FDA reports)
DEHYDRATION ( 33 FDA reports)
HEADACHE ( 33 FDA reports)
CONDITION AGGRAVATED ( 31 FDA reports)
ANAEMIA ( 30 FDA reports)
BRADYCARDIA ( 28 FDA reports)
CEREBROVASCULAR ACCIDENT ( 28 FDA reports)
HYPERKALAEMIA ( 25 FDA reports)
HYPERTENSION ( 25 FDA reports)
PAIN IN EXTREMITY ( 25 FDA reports)
COUGH ( 23 FDA reports)
LOSS OF CONSCIOUSNESS ( 23 FDA reports)
BLOOD CREATININE INCREASED ( 22 FDA reports)
DRUG INEFFECTIVE ( 22 FDA reports)
RECTAL HAEMORRHAGE ( 22 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 20 FDA reports)
MUSCLE SPASMS ( 20 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
CONSTIPATION ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
INJURY ( 18 FDA reports)
SYNCOPE ( 18 FDA reports)
HYPONATRAEMIA ( 17 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 17 FDA reports)
URINARY TRACT INFECTION ( 17 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
PROTEINURIA ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
DISEASE RECURRENCE ( 15 FDA reports)
INSOMNIA ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 14 FDA reports)
HAEMODIALYSIS ( 14 FDA reports)
HEPATITIS C ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
BLOOD PRESSURE INCREASED ( 13 FDA reports)
PARAESTHESIA ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
OLIGURIA ( 11 FDA reports)
PANCYTOPENIA ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
COMA ( 10 FDA reports)
DEATH ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
LACTIC ACIDOSIS ( 10 FDA reports)
LETHARGY ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ALOPECIA ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CHOLECYSTITIS ACUTE ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
ECONOMIC PROBLEM ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PROCTALGIA ( 9 FDA reports)
SHOCK ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
EOSINOPHILIA ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
CATARACT ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HEART INJURY ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
NERVOUSNESS ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
SEDATION ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
AGITATION ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CONTUSION ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HEPATIC HAEMATOMA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
FEAR ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MENTAL IMPAIRMENT ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RASH ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CONGENITAL RENAL CYST ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MICROTIA ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
POISONING ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PURPURA ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RECTOSIGMOID CANCER ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
ULCER ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LEUKOSTASIS ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
POLYP ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SCAR ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URINE ARSENIC INCREASED ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BENIGN BILIARY NEOPLASM ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONGENITAL CYST ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MASS ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROPIONIBACTERIUM INFECTION ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BETA GLOBULIN ABNORMAL ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE RASH ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY CAUDA EQUINA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UROGENITAL PROLAPSE ( 1 FDA reports)
URTICARIA CHOLINERGIC ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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