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

CONDITION AGGRAVATED ( 22 FDA reports)
NAUSEA ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
PYREXIA ( 15 FDA reports)
VOMITING ( 15 FDA reports)
ASTHMA ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
TACHYCARDIA ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
ACIDOSIS ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
NEONATAL DISORDER ( 7 FDA reports)
PAIN ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
FOETAL DISTRESS SYNDROME ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
TACHYCARDIA FOETAL ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
COUGH ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TOXIC NEUROPATHY ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BASE EXCESS ABNORMAL ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMA ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHLEBOTOMUS FEVER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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