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

DYSPNOEA ( 85 FDA reports)
VOMITING ( 45 FDA reports)
ASTHMA ( 44 FDA reports)
RESPIRATORY FAILURE ( 42 FDA reports)
COUGH ( 35 FDA reports)
HYPOTENSION ( 35 FDA reports)
NAUSEA ( 35 FDA reports)
ATRIAL FIBRILLATION ( 34 FDA reports)
DELIRIUM ( 32 FDA reports)
PNEUMONIA ( 31 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 30 FDA reports)
RENAL FAILURE ( 29 FDA reports)
DRUG INEFFECTIVE ( 28 FDA reports)
CONDITION AGGRAVATED ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
FOETAL DISTRESS SYNDROME ( 24 FDA reports)
INSOMNIA ( 24 FDA reports)
MULTI-ORGAN FAILURE ( 24 FDA reports)
HYPERTENSION ( 23 FDA reports)
TACHYCARDIA ( 23 FDA reports)
TACHYCARDIA FOETAL ( 23 FDA reports)
CHEST PAIN ( 21 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 21 FDA reports)
DIARRHOEA ( 21 FDA reports)
METABOLIC ACIDOSIS ( 21 FDA reports)
PAIN ( 21 FDA reports)
WHEEZING ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
SEPSIS ( 20 FDA reports)
ANXIETY ( 19 FDA reports)
DEATH ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 19 FDA reports)
DIZZINESS ( 19 FDA reports)
PLATELET COUNT DECREASED ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
CARDIAC FAILURE ( 18 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
RENAL FAILURE ACUTE ( 18 FDA reports)
RESPIRATORY ARREST ( 18 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
OXYGEN SATURATION DECREASED ( 17 FDA reports)
WEIGHT DECREASED ( 17 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
PALPITATIONS ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
ANAEMIA ( 15 FDA reports)
CHEST DISCOMFORT ( 15 FDA reports)
DISORIENTATION ( 15 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
CYANOSIS ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
MALAISE ( 14 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
CORONARY ARTERY DISEASE ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
GASTRIC ULCER ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
MITRAL VALVE INCOMPETENCE ( 12 FDA reports)
PREMATURE LABOUR ( 12 FDA reports)
PULMONARY HAEMORRHAGE ( 12 FDA reports)
SINUS TACHYCARDIA ( 12 FDA reports)
STATUS EPILEPTICUS ( 12 FDA reports)
ABDOMINAL PAIN UPPER ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
GASTRITIS ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
PRODUCTIVE COUGH ( 11 FDA reports)
RASH ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
ATRIAL FLUTTER ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
DRY MOUTH ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
SHOCK ( 10 FDA reports)
UNEVALUABLE EVENT ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
ANOREXIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
COLITIS ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
DRUG TOXICITY ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
INJURY ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
LUNG INFECTION ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
APNOEA ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TREMOR ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
APHASIA ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
FEAR ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPOAESTHESIA ORAL ( 7 FDA reports)
INFECTION ( 7 FDA reports)
JAUNDICE ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CRYING ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PAROSMIA ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ABDOMINAL SEPSIS ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
APGAR SCORE LOW ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
COSTOCHONDRITIS ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PLEURISY ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
STRESS ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TENSION ( 5 FDA reports)
THIRST ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ARTHROPATHY ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CRANIOSYNOSTOSIS ( 4 FDA reports)
DIABETIC ULCER ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EXOPHTHALMOS CONGENITAL ( 4 FDA reports)
FALL ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HYPERLACTACIDAEMIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALLERGY TEST ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BASE EXCESS ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRACHIAL PULSE INCREASED ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PH BODY FLUID DECREASED ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOPERICARDIUM ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD ZINC INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUTTERING ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HIV INFECTION CDC CATEGORY C3 ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT OBSTRUCTION ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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