COVID-19 vaccine contains the active ingredient(s): Covid-19 vaccine.
Result is presented for the active ingredient(s).
Total number of records retrieved: 2727042

Distribution

Adverse drug reactions (ADRs)

 Blood and lymphatic system disorders (113469)

Lymphadenopathy (87960)

  • Lymph node pain (11213)
  • Thrombocytopenia (7056)
  • Lymphadenitis (2522)
  • Immune thrombocytopenia (2223)
  • Anaemia (2048)
  • Coagulopathy (1030)
  • Leukocytosis (584)
  • Increased tendency to bruise (547)
  • Neutropenia (545)
  • Leukopenia (496)
  • Lymphopenia (416)
  • Spontaneous haematoma (373)
  • Pancytopenia (335)
  • Splenomegaly (301)
  • Disseminated intravascular coagulation (258)
  • Eosinophilia (248)
  • Thrombocytopenic purpura (243)
  • Thrombotic thrombocytopenic purpura (243)
  • Thrombosis with thrombocytopenia syndrome (228)
  • Splenic infarction (214)
  • Autoimmune haemolytic anaemia (213)
  • Iron deficiency anaemia (191)
  • Thrombocytosis (185)
  • Haemolytic anaemia (183)
  • Haemolysis (167)
  • Blood disorder (165)
  • Hypercoagulation (161)
  • Platelet disorder (157)
  • Neutrophilia (138)
  • Antiphospholipid syndrome (131)
  • Hyperleukocytosis (130)
  • Haemorrhagic diathesis (125)
  • White blood cell disorder (114)
  • Lymphadenopathy mediastinal (108)
  • Mast cell activation syndrome (106)
  • Splenic vein thrombosis (100)
  • Acquired haemophilia (99)
  • Normocytic anaemia (89)
  • Nucleated red cells (89)
  • Lymphocytosis (83)
  • Blood loss anaemia (79)
  • Aplastic anaemia (78)
  • Heparin-induced thrombocytopenia (72)
  • Sickle cell anaemia with crisis (71)
  • Agranulocytosis (67)
  • Red blood cell abnormality (67)
  • Haemorrhagic disorder (62)
  • Microcytic anaemia (60)
  • Febrile neutropenia (59)
  • Hilar lymphadenopathy (56)
  • Polycythaemia (55)
  • Thrombotic microangiopathy (52)
  • Lymphatic disorder (46)
  • Spleen disorder (43)
  • Splenic thrombosis (43)
  • Monocytosis (42)
  • Anaemia macrocytic (41)
  • Bicytopenia (41)
  • Abdominal lymphadenopathy (39)
  • Abnormal clotting factor (36)
  • Anisocytosis (35)
  • Spontaneous haemorrhage (34)
  • Bone marrow failure (29)
  • Evans syndrome (29)
  • Myelosuppression (29)
  • Splenic artery thrombosis (29)
  • Anaemia vitamin B12 deficiency (28)
  • Bone marrow disorder (27)
  • Bone marrow oedema (27)
  • Polychromasia (27)
  • Purpura non-thrombocytopenic (27)
  • Cytopenia (26)
  • Pseudolymphoma (24)
  • Activated protein C resistance (20)
  • Hyperfibrinogenaemia (20)
  • Hypofibrinogenaemia (20)
  • Lymphocytic infiltration (20)
  • Necrotic lymphadenopathy (20)
  • Macrocytosis (19)
  • Mastocytosis (19)
  • Pernicious anaemia (19)
  • Hypochromic anaemia (18)
  • Paratracheal lymphadenopathy (17)
  • Autoimmune neutropenia (16)
  • Haemoglobinaemia (16)
  • Warm type haemolytic anaemia (16)
  • Cold type haemolytic anaemia (15)
  • Haemolytic uraemic syndrome (15)
  • Hypereosinophilic syndrome (15)
  • Hypergammaglobulinaemia (15)
  • Microangiopathic haemolytic anaemia (15)
  • Normochromic normocytic anaemia (15)
  • Platelet anisocytosis (15)
  • Aplasia pure red cell (14)
  • Factor VIII inhibition (14)
  • Hypochromasia (14)
  • Autoimmune anaemia (13)
  • Coombs positive haemolytic anaemia (12)
  • Anaemia folate deficiency (11)
  • Atypical haemolytic uraemic syndrome (11)
  • Lymphoid tissue hyperplasia (11)
  • Splenic haemorrhage (11)
  • Coombs negative haemolytic anaemia (10)
  • Retroperitoneal lymphadenopathy (10)
  • Bandaemia (9)
  • Hypocoagulable state (9)
  • Thymus disorder (9)
  • Thymus enlargement (9)
  • Elliptocytosis (8)
  • Haemoconcentration (8)
  • Lymphatic obstruction (8)
  • Normochromic anaemia (8)
  • Schistocytosis (8)
  • Anaemia of chronic disease (7)
  • Lymphatic insufficiency (7)
  • Poikilocytosis (7)
  • Splenic embolism (7)
  • Acquired Von Willebrand’s disease (6)
  • Eosinopenia (6)
  • Granulomatous lymphadenitis (6)
  • Lymph node calcification (6)
  • Methaemoglobinaemia (6)
  • Microcytosis (6)
  • Monoclonal B-cell lymphocytosis (6)
  • Monocytopenia (6)
  • Spontaneous heparin-induced thrombocytopenia syndrome (6)
  • Erythropenia (5)
  • Granulocytopenia (5)
  • Reticulocytosis (5)
  • Splenic cyst (5)
  • Splenic lesion (5)
  • Anaemia megaloblastic (4)
  • Erythropoiesis abnormal (4)
  • Febrile bone marrow aplasia (4)
  • Hyperviscosity syndrome (4)
  • Hypoplastic anaemia (4)
  • Lymph node rupture (4)
  • Spleen ischaemia (4)
  • Splenic varices (4)
  • Splenic vein occlusion (4)
  • Acquired factor VIII deficiency (3)
  • Autoimmune pancytopenia (3)
  • Basophilia (3)
  • Coagulation disorder neonatal (3)
  • Deficiency anaemia (3)
  • Disseminated intravascular coagulation in newborn (3)
  • Elephantiasis (3)
  • Hyperchromic anaemia (3)
  • Jaundice acholuric (3)
  • Lymph node haemorrhage (3)
  • Nephrogenic anaemia (3)
  • Placental transfusion syndrome (3)
  • Platelet destruction increased (3)
  • Post-anaphylaxis mast cell anergy (3)
  • Red blood cell agglutination (3)
  • Splenic calcification (3)
  • Splenitis (3)
  • Stress polycythaemia (3)
  • Acquired dysfibrinogenaemia (2)
  • Autoimmune heparin-induced thrombocytopenia (2)
  • Bone marrow infiltration (2)
  • Bone marrow reticulin fibrosis (2)
  • Breakthrough haemolysis (2)
  • Eosinophilia myalgia syndrome (2)
  • Extramedullary haemopoiesis (2)
  • Factor V inhibition (2)
  • Foetal anaemia (2)
  • Granulocytosis (2)
  • Heparin resistance (2)
  • Hyperfibrinolysis (2)
  • Hypoprothrombinaemia (2)
  • Intravascular haemolysis (2)
  • Isoimmune haemolytic disease (2)
  • Leukaemoid reaction (2)
  • Lymph node ulcer (2)
  • Platelet dysfunction (2)
  • Secondary thrombocytosis (2)
  • Spherocytic anaemia (2)
  • Spleen atrophy (2)
  • Splenic artery stenosis (2)
  • Splenic granuloma (2)
  • Splenic necrosis (2)
  • Subcapsular splenic haematoma (2)
  • Acquired amegakaryocytic thrombocytopenia (1)
  • Anaemia of malignant disease (1)
  • Anisochromia (1)
  • Basophilopenia (1)
  • B-lymphocyte abnormalities (1)
  • Bone marrow ischaemia (1)
  • Bone marrow oedema syndrome (1)
  • Clonal haematopoiesis (1)
  • Coagulation factor deficiency (1)
  • Cutaneous extramedullary haemopoiesis (1)
  • Dysglobulinaemia (1)
  • Erythroblastosis (1)
  • Factor XIII Inhibition (1)
  • Granulocytes maturation arrest (1)
  • Heinz bodies (1)
  • Hyperplasia of thymic epithelium (1)
  • Hyperprothrombinaemia (1)
  • Hypersplenism (1)
  • Hyperthrombinaemia (1)
  • Hyposplenism (1)
  • Idiopathic CD4 lymphocytopenia (1)
  • Idiopathic neutropenia (1)
  • Leukoerythroblastic anaemia (1)
  • Leukostasis syndrome (1)
  • Lupus anticoagulant hypoprothrombinaemia syndrome (1)
  • Lymph node fibrosis (1)
  • Lymphadenocyst (1)
  • Myelocytosis (1)
  • Myeloid maturation arrest (1)
  • Neutropenia neonatal (1)
  • Neutrophil function disorder (1)
  • Plasmacytosis (1)
  • Platelet production decreased (1)
  • Polyclonal B-cell lymphocytosis (1)
  • Punctate basophilia (1)
  • Pure white cell aplasia (1)
  • Red blood cell vacuolisation (1)
  • Red cell fragmentation syndrome (1)
  • Reticuloendothelial system stimulated (1)
  • Rouleaux formation (1)
  • Spleen congestion (1)
  • Splenorenal shunt (1)

 Cardiac disorders (150250)

  • Palpitations (48942)
  • Tachycardia (34735)
  • Myocarditis (14496)
  • Pericarditis (11096)
  • Arrhythmia (9881)
  • Atrial fibrillation (7164)
  • Myocardial infarction (5155)
  • Angina pectoris (4856)
  • Cardiac arrest (3286)
  • Bradycardia (2880)
  • Cardiac failure (2716)
  • Cardiac flutter (2703)
  • Acute myocardial infarction (2585)
  • Cardiovascular disorder (2447)
  • Extrasystoles (2348)
  • Pericardial effusion (2157)
  • Cardiac disorder (1874)
  • Ventricular extrasystoles (1418)
  • Sinus tachycardia (1363)
  • Cardio-respiratory arrest (1191)
  • Cardiac discomfort (1093)
  • Supraventricular tachycardia (895)
  • Cardiomegaly (752)
  • Cardiac failure congestive (751)
  • Atrial flutter (663)
  • Acute coronary syndrome (627)
  • Ventricular tachycardia (524)
  • Ventricular fibrillation (459)
  • Cardiomyopathy (444)
  • Cardiogenic shock (425)
  • Coronary artery disease (419)
  • Cardiac failure acute (417)
  • Supraventricular extrasystoles (410)
  • Postural orthostatic tachycardia syndrome (358)
  • Myocardial ischaemia (318)
  • Atrioventricular block (310)
  • Mitral valve incompetence (307)
  • Left ventricular dysfunction (288)
  • Bundle branch block right (275)
  • Sinus bradycardia (274)
  • Coronary artery occlusion (265)
  • Intracardiac thrombus (260)
  • Tachyarrhythmia (258)
  • Coronary artery thrombosis (250)
  • Cardiac fibrillation (247)
  • Atrioventricular block complete (228)
  • Stress cardiomyopathy (201)
  • Congestive cardiomyopathy (200)
  • Pulseless electrical activity (200)
  • Tricuspid valve incompetence (194)
  • Ventricular hypokinesia (189)
  • Bundle branch block left (174)
  • Carditis (171)
  • Cardiac tamponade (160)
  • Sinus arrhythmia (160)
  • Left ventricular failure (151)
  • Left ventricular hypertrophy (150)
  • Arteriosclerosis coronary artery (149)
  • Coronary artery stenosis (144)
  • Atrial tachycardia (136)
  • Cardiovascular insufficiency (134)
  • Myocardial injury (134)
  • Angina unstable (131)
  • Cardiac dysfunction (129)
  • Atrioventricular block second degree (117)
  • Cardiac failure chronic (108)
  • Atrioventricular block first degree (107)
  • Pleuropericarditis (106)
  • Cardiopulmonary failure (105)
  • Aortic valve incompetence (103)
  • Arrhythmia supraventricular (100)
  • Tachycardia paroxysmal (97)
  • Right ventricular failure (96)
  • Cardiac ventricular thrombosis (88)
  • Coronary artery dissection (88)
  • Ventricular arrhythmia (86)
  • Diastolic dysfunction (85)
  • Hypertensive heart disease (84)
  • Right ventricular dysfunction (82)
  • Myocardial oedema (77)
  • Cardiovascular symptom (75)
  • Acute left ventricular failure (73)
  • Heart valve incompetence (71)
  • Myocardial fibrosis (66)
  • Right ventricular dilatation (61)
  • Cardiac valve disease (60)
  • Pericardial haemorrhage (60)
  • Arteriospasm coronary (58)
  • Mitral valve prolapse (58)
  • Sinus node dysfunction (53)
  • Acute cardiac event (52)
  • Atrial thrombosis (52)
  • Cor pulmonale acute (50)
  • Chronic left ventricular failure (48)
  • Left atrial enlargement (48)
  • Pericardial fibrosis (48)
  • Ventricular hypertrophy (45)
  • Bundle branch block (44)
  • Left ventricular dilatation (44)
  • Ventricular dysfunction (43)
  • Sinus arrest (42)
  • Systolic dysfunction (42)
  • Cardiac hypertrophy (39)
  • Left atrial dilatation (39)
  • Atrial enlargement (38)
  • Ischaemic cardiomyopathy (38)
  • Cor pulmonale (37)
  • Aortic valve stenosis (35)
  • Cardiac aneurysm (33)
  • Prinzmetal angina (30)
  • Conduction disorder (28)
  • Heart alternation (27)
  • Myocardial rupture (27)
  • Pericardial disease (27)
  • Pericardial rub (27)
  • Pericarditis constrictive (27)
  • Right ventricular enlargement (27)
  • Myocardial necrosis (26)
  • Right atrial dilatation (26)
  • Tachycardia foetal (26)
  • Nodal rhythm (25)
  • Foetal cardiac arrest (23)
  • Pulmonary valve incompetence (23)
  • Right atrial enlargement (23)
  • Bradyarrhythmia (22)
  • Coronary artery embolism (21)
  • Left ventricular enlargement (21)
  • Right ventricular hypertrophy (21)
  • Aortic valve calcification (19)
  • Cardiac asthma (19)
  • Dilatation atrial (19)
  • Hyperdynamic left ventricle (17)
  • Mitral valve calcification (16)
  • Supraventricular tachyarrhythmia (15)
  • Torsade de pointes (15)
  • Cardiac sarcoidosis (14)
  • Dilatation ventricular (14)
  • Mitral valve disease (14)
  • Nodal arrhythmia (14)
  • Aortic valve sclerosis (13)
  • Cardiac septal hypertrophy (13)
  • Cardio-respiratory distress (13)
  • Defect conduction intraventricular (13)
  • Brugada syndrome (12)
  • Microvascular coronary artery disease (12)
  • Paroxysmal arrhythmia (12)
  • Ventricular enlargement (12)
  • Wolff-Parkinson-White syndrome (12)
  • Bradycardia foetal (11)
  • Coronary artery dilatation (11)
  • Mitral valve stenosis (11)
  • Ventricular dyskinesia (11)
  • Ventricular tachyarrhythmia (11)
  • Cardiac ventricular disorder (10)
  • Dressler’s syndrome (10)
  • Long QT syndrome (10)
  • Aortic valve disease (9)
  • Cardiomyopathy acute (9)
  • Eosinophilic myocarditis (9)
  • Mitral valve thickening (9)
  • Paroxysmal atrioventricular block (9)
  • Sinoatrial block (9)
  • Ventricular failure (9)
  • Aortic valve thickening (8)
  • Arrhythmia neonatal (8)
  • Autoimmune myocarditis (8)
  • Bifascicular block (8)
  • Cardiac perfusion defect (8)
  • Cardiorenal syndrome (8)
  • Agonal rhythm (7)
  • Coronary artery aneurysm (7)
  • Low cardiac output syndrome (7)
  • Myocardial hypoxia (7)
  • Silent myocardial infarction (7)
  • Tachycardia induced cardiomyopathy (7)
  • Arrhythmic storm (6)
  • Cardiac amyloidosis (6)
  • Cardiovascular deconditioning (6)
  • Hepatojugular reflux (6)
  • Hypertensive cardiomyopathy (6)
  • Immune-mediated myocarditis (6)
  • Kounis syndrome (6)
  • Tricuspid valve disease (6)
  • Bundle branch block bilateral (5)
  • Chordae tendinae rupture (5)
  • Coronary ostial stenosis (5)
  • Interventricular septum rupture (5)
  • Intracardiac mass (5)
  • Pulmonary valve stenosis (5)
  • Restrictive cardiomyopathy (5)
  • Rhythm idioventricular (5)
  • Ventricular dyssynchrony (5)
  • Heart valve calcification (4)
  • Hypersensitivity myocarditis (4)
  • Pericardial cyst (4)
  • Pericardial mass (4)
  • Pneumopericardium (4)
  • Pulmonary valve disease (4)
  • Trifascicular block (4)
  • Accelerated idioventricular rhythm (3)
  • Adams-Stokes syndrome (3)
  • Cardiac valve sclerosis (3)
  • Cardiomyopathy neonatal (3)
  • Endocarditis noninfective (3)
  • Foetal heart rate disorder (3)
  • Gastrocardiac syndrome (3)
  • Giant cell myocarditis (3)
  • Heart valve stenosis (3)
  • Myocardial depression (3)
  • Pulmonary valve thickening (3)
  • Right ventricular diastolic collapse (3)
  • Ventricle rupture (3)
  • Ventricular flutter (3)
  • Acute right ventricular failure (2)
  • Arteritis coronary (2)
  • Atrioventricular node dysfunction (2)
  • Cardiac steatosis (2)
  • Cardiac valve thickening (2)
  • Cardiomyopathy alcoholic (2)
  • Chronic coronary syndrome (2)
  • Degenerative aortic valve disease (2)
  • Degenerative mitral valve disease (2)
  • Endocardial disease (2)
  • Foetal arrhythmia (2)
  • Foetal heart rate acceleration abnormality (2)
  • Foetal heart rate deceleration abnormality (2)
  • Intrapericardial thrombosis (2)
  • Myocardial haemorrhage (2)
  • Papillary muscle rupture (2)
  • Rheumatic heart disease (2)
  • Right ventricular hypertension (2)
  • Sigmoid-shaped ventricular septum (2)
  • Toxic cardiomyopathy (2)
  • Wandering pacemaker (2)
  • Abnormal precordial movement (1)
  • Acquired cardiac septal defect (1)
  • Anginal equivalent (1)
  • Atrioventricular conduction time shortened (1)
  • Atrioventricular dissociation (1)
  • Bezold-Jarisch reflex (1)
  • Cardiac arrest neonatal (1)
  • Cardiac perforation (1)
  • Cardiac valve discolouration (1)
  • Cardiotoxicity (1)
  • Coronary artery perforation (1)
  • Early repolarisation syndrome (1)
  • Hypertensive cardiomegaly (1)
  • Ischaemic mitral regurgitation (1)
  • Lupus endocarditis (1)
  • Malignant hypertensive heart disease (1)
  • Myocardial stunning (1)
  • Myocarditis post infection (1)
  • Neonatal tachycardia (1)
  • Obesity cardiomyopathy (1)
  • Parasystole (1)
  • Pericarditis adhesive (1)
  • Pericarditis rheumatic (1)
  • Pericarditis uraemic (1)
  • Postinfarction angina (1)
  • Sinusoidal foetal heart rate pattern (1)
  • Tricuspid valve prolapse (1)
  • Ventricular hyperkinesia (1)
  • Ventricular remodelling (1)

 Congenital, familial and genetic disorders (1621)

  • Factor V Leiden mutation (93)
  • Atrial septal defect (85)
  • Heart disease congenital (61)
  • Factor II mutation (58)
  • Hypertrophic cardiomyopathy (43)
  • Macroglossia (42)
  • Colour blindness (37)
  • Ehlers-Danlos syndrome (37)
  • Cerebral palsy (32)
  • Gene mutation (32)
  • Congenital anomaly (29)
  • Tourette’s disorder (29)
  • Foetal malformation (23)
  • Arnold-Chiari malformation (22)
  • Hydrocele (21)
  • Factor VIII deficiency (20)
  • Hereditary angioedema (19)
  • Arteriovenous malformation (18)
  • Methylenetetrahydrofolate reductase gene mutation (18)
  • Trisomy 21 (18)
  • Gilbert’s syndrome (17)
  • Paroxysmal extreme pain disorder (17)
  • Ventricular septal defect (16)
  • Dermoid cyst (15)
  • Haemophilia (15)
  • Anencephaly (14)
  • Dysmorphism (13)
  • Factor V Leiden carrier (12)
  • Familial mediterranean fever (12)
  • Huntington’s disease (12)
  • Corneal dystrophy (11)
  • Janus kinase 2 mutation (11)
  • Bicuspid aortic valve (10)
  • Limb malformation (10)
  • Limb reduction defect (10)
  • Muscular dystrophy (10)
  • Syringomyelia (10)
  • Von Willebrand’s disease (10)
  • Congenital central nervous system anomaly (9)
  • Congenital cystic kidney disease (9)
  • Cystic lymphangioma (9)
  • Micropenis (9)
  • Spina bifida (9)
  • Venous angioma of brain (9)
  • Ankyloglossia congenital (8)
  • Antithrombin III deficiency (8)
  • Cytogenetic abnormality (8)
  • Porphyria (8)
  • Retinitis pigmentosa (8)
  • Trisomy 18 (8)
  • Vascular malformation (8)
  • Cerebral cavernous malformation (7)
  • Foetal chromosome abnormality (7)
  • Foetal cystic hygroma (7)
  • Methylmalonic aciduria (7)
  • Porphyria acute (7)
  • Type V hyperlipidaemia (7)
  • Xeroderma pigmentosum (7)
  • Birth mark (6)
  • Branchial cyst (6)
  • Congenital hearing disorder (6)
  • Cystic fibrosis (6)
  • Factor V deficiency (6)
  • Familial hemiplegic migraine (6)
  • Familial periodic paralysis (6)
  • Gastroschisis (6)
  • Glucose-6-phosphate dehydrogenase deficiency (6)
  • Hereditary ataxia (6)
  • Hereditary neuropathy with liability to pressure palsies (6)
  • Myocardial bridging (6)
  • Myoclonic dystonia (6)
  • Phimosis (6)
  • Thyroglossal cyst (6)
  • Aplasia (5)
  • Cleft lip (5)
  • Cleft lip and palate (5)
  • Factor VII deficiency (5)
  • Haemorrhagic arteriovenous malformation (5)
  • Hyperglycinaemia (5)
  • Kidney malformation (5)
  • Macrocephaly (5)
  • Malformation venous (5)
  • Multiple congenital abnormalities (5)
  • Protein S deficiency (5)
  • Renal dysplasia (5)
  • Single umbilical artery (5)
  • Trisomy 13 (5)
  • Vestibulocerebellar syndrome (5)
  • Alpha-1 antitrypsin deficiency (4)
  • Amegakaryocytic thrombocytopenia (4)
  • CALR gene mutation (4)
  • Cleft palate (4)
  • Combined immunodeficiency (4)
  • Congenital hydrocephalus (4)
  • Encephalocele (4)
  • Epidermolysis bullosa (4)
  • Gastrointestinal malformation (4)
  • Hereditary motor and sensory neuropathy (4)
  • Hereditary spherocytosis (4)
  • Heterotaxia (4)
  • Hyperexplexia (4)
  • Hypoplastic left heart syndrome (4)
  • Kidney duplex (4)
  • Laryngomalacia (4)
  • MPL gene mutation (4)
  • Naevus flammeus (4)
  • Neurofibromatosis (4)
  • Pectus excavatum (4)
  • Protein C deficiency (4)
  • Sickle cell anaemia (4)
  • Spine malformation (4)
  • Thalassaemia (4)
  • Thalassaemia minor (4)
  • Transposition of the great vessels (4)
  • Type IIa hyperlipidaemia (4)
  • Ventricular hypoplasia (4)
  • Vertebral artery hypoplasia (4)
  • Accessory spleen (3)
  • Benign familial pemphigus (3)
  • Block vertebra (3)
  • BRAF gene mutation (3)
  • Bronchogenic cyst (3)
  • Cardiac septal defect (3)
  • Cerebrovascular arteriovenous malformation (3)
  • Coarctation of the aorta (3)
  • Congenital absence of cranial vault (3)
  • Congenital arterial malformation (3)
  • Congenital cerebrovascular anomaly (3)
  • Congenital diaphragmatic hernia (3)
  • Congenital great vessel anomaly (3)
  • Congenital jaw malformation (3)
  • Congenital myopathy (3)
  • Congenital uterine anomaly (3)
  • Craniosynostosis (3)
  • Cryopyrin associated periodic syndrome (3)
  • Fallot’s tetralogy (3)
  • Glycogen storage disease type V (3)
  • Hyper IgD syndrome (3)
  • Keratosis follicular (3)
  • Left-to-right cardiac shunt (3)
  • MELAS syndrome (3)
  • Mitral valve atresia (3)
  • Patent ductus arteriosus (3)
  • Penoscrotal fusion (3)
  • Porencephaly (3)
  • Preauricular cyst (3)
  • Renal fusion anomaly (3)
  • Spinal muscular atrophy (3)
  • Supernumerary nipple (3)
  • Syndactyly (3)
  • Turner’s syndrome (3)
  • Aberrant aortic arch (2)
  • Adrenogenital syndrome (2)
  • Anomalous pulmonary venous connection (2)
  • Argininosuccinate lyase deficiency (2)
  • Arrhythmogenic right ventricular dysplasia (2)
  • Asplenia (2)
  • Asymmetric crying facies (2)
  • Ataxia telangiectasia (2)
  • Atrioventricular septal defect (2)
  • Brachyolmia (2)
  • Cerebellar hypoplasia (2)
  • Cerebral arteriovenous malformation haemorrhagic (2)
  • CFTR gene mutation (2)
  • Chimerism (2)
  • Congenital cystic lung (2)
  • Congenital heart valve disorder (2)
  • Congenital inguinal hernia (2)
  • Congenital methaemoglobinaemia (2)
  • Congenital myasthenic syndrome (2)
  • Congenital skin dimples (2)
  • Congenital thrombocyte disorder (2)
  • Conjoined twins (2)
  • Cryptorchism (2)
  • CYP2C19 polymorphism (2)
  • Dacryostenosis congenital (2)
  • Developmental hip dysplasia (2)
  • Dextrocardia (2)
  • Diastematomyelia (2)
  • Duchenne muscular dystrophy gene carrier (2)
  • EGFR gene mutation (2)
  • Elliptocytosis hereditary (2)
  • Epilepsy with myoclonic-atonic seizures (2)
  • Exomphalos (2)
  • Factor XIII deficiency (2)
  • Galactosialidosis (2)
  • Gastrointestinal arteriovenous malformation (2)
  • Grey matter heterotopia (2)
  • Hereditary haemorrhagic telangiectasia (2)
  • Ichthyosis (2)
  • Intestinal atresia (2)
  • Intracranial lipoma (2)
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 Ear and labyrinth disorders (90060)

  • Vertigo (35352)
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 Endocrine disorders (4472)

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 Eye disorders (99734)

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 Gastrointestinal disorders (538499)

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 General disorders and administration site conditions (1629961)

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 Hepatobiliary disorders (5831)

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 Immune system disorders (43673)

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 Infections and infestations (215663)

  • COVID-19 (74259)
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 Injury, poisoning and procedural complications (148474)

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 Investigations (387796)

  • SARS-CoV-2 test (79667)
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 Metabolism and nutrition disorders (60306)

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 Product issues (4221)

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 Psychiatric disorders (127483)

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 Renal and urinary disorders (22836)

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 Respiratory, thoracic and mediastinal disorders (290927)

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 Surgical and medical procedures (34122)

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 Vascular disorders (144967)

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