MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Infantile Colic

(UMLS:C0266836)

UMLS ID:: C0266836
MeSH ID:: D003085

Classification:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.614.166

Synonym(s)

Infantile Colic

Colic

Colic, infantile

Infant Colic

Infantile colic

Infantile colic - symptom

Three month colic

colic infant

colic infantile

10.

colic infants

11.

colic; infantile

12.

colics infantile

13.

infant colic

14.

infant; colic

15.

infantile colic

Associated Drug(s)

	Name	Number of Reports	Data Source
1	Metronidazole	FAERS: 6	US FAERS
2	Fluoxetine	FAERS: 3	US FAERS
3	Norgestrel	FAERS: 2 Canada Vigilance: 1	Canada Vigilance OFFSIDES US FAERS
4	Propranolol	FAERS: 1	US FAERS
5	Quetiapine Fumarate	FAERS: 1	US FAERS
6	Norethindrone	Canada Vigilance: 1	Canada Vigilance
7	Sulfate		OFFSIDES
8	Terbutaline		OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Amniotic Band Syndrome	42.9%
2	Asphyxia Neonatorum	42.9%
3	Infant, Premature, Diseases	42.9%
4	Anemia, Neonatal	27.9%
5	Persistent Fetal Circulation Syndrome	27.9%
6	Umbilical hernia	27.4%
7	Deformity	23.1%
8	Genetic Diseases, Inborn	23.1%
9	Cystic Fibrosis	22.9%
10	Neonatal Abstinence Syndrome	21.4%
11	Paralysis, Obstetric	20.9%
12	Retinopathy of Prematurity	20.9%
13	Xeroderma	20.5%
14	Mobius Syndrome	20.5%
15	Congenital nystagmus	20.5%
16	Toxoplasmosis, Congenital	20.3%
17	Bronchopulmonary Dysplasia	20.2%
18	Syphilis, Congenital	20.2%
19	Meconium Aspiration Syndrome	18.6%
20	Congenital Hyperinsulinism	16.4%
21	Respiratory Distress Syndrome, Newborn	15.8%
22	Beckwith-Wiedemann Syndrome	15.3%
23	Wolf-Hirschhorn Syndrome	15.3%
24	Fetal Diseases	15%
25	Abnormalities, Drug-Induced	14.3%
26	Situs Inversus	14.3%
27	Ichthyosis, X-Linked	13.2%
28	Hyaline Membrane Disease	12.6%
29	Smith-Magenis syndrome	12.3%
30	Aicardi's syndrome	12.2%
31	Cri-du-Chat Syndrome	12.1%
32	Down Syndrome	12.1%
33	Trisomy 21	12.1%
34	CHARGE Syndrome	12.1%
35	Leukomalacia, Periventricular	12%
36	Nesidioblastosis	11.9%
37	Holoprosencephaly	11.7%
38	Hyperkeratosis, Epidermolytic	11.4%
39	Ophthalmia Neonatorum	11.3%
40	Sjogren-Larsson Syndrome	11%
41	Fragile X Syndrome	10.9%
42	Familial Mediterranean Fever	10.3%
43	Prune Belly Syndrome	10.3%
44	Twins, Conjoined	10.3%
45	Waardenburg Syndrome	10.3%
46	Ectodermal Dysplasia	10.1%
47	Aplasia Cutis Congenita	10.1%
48	Eye Abnormalities	10%
49	Neoplastic Syndromes, Hereditary	10%
50	Prader-Willi Syndrome	10%
51	Cardiovascular Abnormalities	10%
52	Nail-Patella Syndrome	9.7%
53	Rubinstein-Taybi Syndrome	9.5%
54	Skin Abnormalities	9.5%
55	Lymphatic Abnormalities	9.5%
56	Congenital Microtia	9.5%
57	Multiple Epiphyseal Dysplasia	9.3%
58	Osteochondrodysplasias	9.3%
59	Pelger-Huet Anomaly	9.3%
60	Werner Syndrome	9.3%
61	Myasthenic Syndromes, Congenital	9.3%
62	Anencephaly	9.2%
63	Congenital diaphragmatic hernia	9.2%
64	Kernicterus	8.7%
65	Cockayne Syndrome	8.6%
66	Alstrom Syndrome	8.5%
67	Kartagener Syndrome	8.5%
68	Rett Syndrome	8.2%
69	Marfan Syndrome	8.1%
70	Primary Ciliary Dyskinesia	8%
71	Anemia, Sickle Cell	8%
72	Thalassemia	8%
73	Muscular Dystrophy, Duchenne	8%
74	Polycystic Kidney Diseases	8%
75	Williams Syndrome	8%
76	Smith-Lemli-Opitz Syndrome	7.5%
77	Maxillofacial Abnormalities	7.5%
78	Dural Arteriovenous Fistula	7.5%
79	Classical Lissencephalies and Subcortical Band Heterotopias	7.4%
80	Urogenital Abnormalities	7.4%
81	Dextrocardia	7.4%
82	Dwarfism	7.3%
83	Albinism	7.1%
84	Anophthalmos	7%
85	Anus, Imperforate	7%
86	Hydranencephaly	7%
87	Microphthalmos	7%
88	Neural Tube Defects	7%
89	Retinal Dysplasia	7%
90	Tethered Cord Syndrome	7%
91	Iniencephaly	7%
92	Craniorachischisis	7%
93	Limb Deformities, Congenital	7%
94	Exencephaly	7%
95	Septo-Optic Dysplasia	7%
96	Craniofacial Abnormalities	7%
97	Cortical Dysplasia	7%
98	Malformations of Cortical Development	7%
99	Anorectal Malformations	7%
100	Aniridia	6.9%
101	Fetal Growth Retardation	6.9%
102	Muscular Dystrophy	6.8%
103	Osteogenesis Imperfecta	6.8%
104	Fetal Hypoxia	6.8%
105	Fetal Alcohol Spectrum Disorders	6.8%
106	Mucopolysaccharidosis II	6.8%
107	Amino Acid Metabolism, Inborn Errors	6.8%
108	Bloom Syndrome	6.8%
109	Carbohydrate Metabolism, Inborn Errors	6.8%
110	Metal Metabolism, Inborn Errors	6.8%
111	Progeria	6.8%
112	Lysosomal Storage Diseases	6.8%
113	Cytochrome-c Oxidase Deficiency	6.8%
114	Peroxisomal Disorders	6.8%
115	Epidermolysis Bullosa	6.7%
116	Sickle Cell Trait	6.5%
117	Polycystic Kidney, Autosomal Dominant	6.5%
118	Microcephaly	6.3%
119	Macrocephaly	6.3%
120	Kallmann Syndrome	5.9%
121	Menkes Kinky Hair Syndrome	5.9%
122	Porencephaly	5.9%
123	Neuronal Ceroid-Lipofuscinoses	5.8%
124	Wiskott-Aldrich Syndrome	5.7%
125	Tuberous Sclerosis	5.6%
126	Amelia	5.6%
127	Arachnodactyly	5.6%
128	Ectopia Cordis	5.6%
129	Ectromelia	5.6%
130	Hemimelia	5.6%
131	Meningomyelocele	5.6%
132	Phocomelia	5.6%
133	Sirenomelia	5.6%
134	Spina Bifida	5.6%
135	Polydactyly	5.6%
136	Brachydactyly	5.6%
137	Plagiocephaly	5.6%
138	Lower Extremity Deformities, Congenital	5.6%
139	Upper Extremity Deformities, Congenital	5.6%
140	Single umbilical artery	5.6%
141	Alkaptonuria	5.6%
142	Glycogen Storage Disease	5.6%
143	Hypophosphatasia	5.6%
144	Propionic acidemia	5.6%
145	Autoimmune Lymphoproliferative Syndrome	5.6%
146	Dihydropyrimidine Dehydrogenase Deficiency	5.6%
147	Cystinosis	5.6%
148	Craniosynostosis	5.5%
149	Syndactyly	5.5%
150	Brachycephaly	5.5%
151	Klinefelter Syndrome	5.5%
152	Charcot-Marie-Tooth Disease	5.5%
153	Antley-Bixler Syndrome Phenotype	5.5%
154	Chorioamnionitis	5.4%
155	Refsum Disease	5.4%
156	Scimitar Syndrome	5.4%
157	Angioedemas, Hereditary	5.4%
158	Turner Syndrome	5.3%
159	Acrocephalosyndactylia	5.3%
160	Blepharophimosis	5.3%
161	Laryngostenosis	5.3%
162	Mouth Abnormalities	5.3%
163	Cutis Laxa	5.2%
164	Esophageal Atresia	5.2%
165	Intestinal Atresia	5.2%
166	Horseshoe Kidney	5.2%
167	Pectus excavatum	5.2%
168	Klippel-Feil Syndrome	5.1%
169	Retinitis Pigmentosa	5.1%
170	Gastroschisis	5.1%
171	Synostosis	5.1%
172	Pigmentary retinopathy	5.1%
173	Acrodermatitis	5.1%
174	Lymphangiectasis, Intestinal	5.1%
175	Porokeratosis	5.1%
176	Gianotti-Crosti Syndrome	5.1%
177	Keratoderma, Palmoplantar	5.1%
178	Pseudoxanthoma Elasticum	5.1%
179	Chronic granulomatous disease	5%
180	Welander Distal Myopathy	5%
181	Dermal Sinus	5%
182	Spina Bifida Cystica	5%
183	Spina Bifida Occulta	5%
184	Lissencephaly	5%
185	Polymicrogyria	5%
186	Pachygyria	5%
187	Schizencephaly	5%
188	Periventricular Nodular Heterotopia	5%
189	Myotonic Dystrophy	5%
190	Glycogen Storage Disease Type I	4.9%
191	Glycogen Storage Disease Type V	4.9%
192	Poland Syndrome	4.9%
193	Mucopolysaccharidosis III	4.9%
194	Glycogen storage disease type II	4.8%
195	Noonan Syndrome	4.8%
196	Zellweger Syndrome	4.8%
197	Acute Chest Syndrome	4.8%
198	Galactosemias	4.7%
199	Urea Cycle Disorders, Inborn	4.7%
200	Tyrosinemias	4.7%
201	Adrenoleukodystrophy	4.7%
202	Fabry Disease	4.6%
203	Jaw Abnormalities	4.6%
204	Cleft Palate	4.5%
205	Xeroderma Pigmentosum	4.5%
206	Amyloid Neuropathies, Familial	4.5%
207	Abnormalities, Radiation-Induced	4.5%
208	Hepatolenticular Degeneration	4.4%
209	Hydrops Fetalis	4.4%
210	Arthrogryposis	4.2%
211	Choanal Atresia	4.2%
212	Tracheobronchomegaly	4.2%
213	Laryngocele	4.2%
214	Aortic coarctation	4.2%
215	Cor Triatriatum	4.2%
216	Coronary Vessel Anomalies	4.2%
217	Dental Enamel Hypoplasia	4.2%
218	Patent ductus arteriosus	4.2%
219	Ebstein Anomaly	4.2%
220	Heart Septal Defects	4.2%
221	Hypodontia	4.2%
222	Macrostomia	4.2%
223	Meningocele	4.2%
224	Microstomia	4.2%
225	Tetralogy of Fallot	4.2%
226	Transposition of Great Vessels	4.2%
227	Hypoplastic Left Heart Syndrome	4.2%
228	May-Thurner Syndrome	4.2%
229	Encephalocele	4.2%
230	Choledochal Cyst	4.2%
231	Craniofacial Dysostosis	4.2%
232	Duane Retraction Syndrome	4.2%
233	Hermaphroditism	4.2%
234	Disorders of Sex Development	4.2%
235	Hypolipoproteinemias	4.1%
236	Papillon-Lefevre Disease	4.1%
237	Wolff-Parkinson-White Syndrome	4.1%
238	Hyperlipidemia, Familial Combined	4.1%
239	Cryptorchidism	4.1%
240	Porphyrias, Hepatic	4.1%
241	Hypospadias	4.1%
242	Hyperlipoproteinemia Type III	4.1%
243	Optic Atrophy, Hereditary, Leber	4.1%
244	Micrognathism	4.1%
245	Pierre Robin Syndrome	4.1%
246	Central Nervous System Cysts	4.1%
247	Hyperphosphaturia	4.1%
248	Gaucher Disease	4.1%
249	Dandy-Walker Syndrome	4.1%
250	Peutz-Jeghers Syndrome	4%
251	Myotonia Congenita	4%
252	Thrombasthenia	4%
253	Antithrombin III Deficiency	4%
254	Protein C Deficiency	4%
255	Brain Diseases, Metabolic, Inborn	4%
256	Afibrinogenemia	4%
257	Dystonia Musculorum Deformans	4%
258	Factor VII Deficiency	4%
259	Factor X Deficiency	4%
260	Factor XII Deficiency	4%
261	Hemophilia A	4%
262	POEMS Syndrome	4%
263	Activated Protein C Resistance	4%
264	Factor II deficiency	4%
265	Factor VIII Deficiency	4%
266	Factor V deficiency	4%
267	Factor XI Deficiency	4%
268	Hypoprothrombinemias	4%
269	Fanconi Anemia	4%
270	Basal Cell Nevus Syndrome	4%
271	Lafora Disease	4%
272	Unverricht-Lundborg Syndrome	4%
273	Anemia, Diamond-Blackfan	3.9%
274	Homocystinuria	3.9%
275	Leigh Disease	3.9%
276	Tay-Sachs Disease	3.9%
277	Canavan Disease	3.8%
278	Alexander Disease	3.8%
279	Aortopulmonary Septal Defect	3.7%
280	Double Outlet Right Ventricle	3.7%
281	Endocardial Cushion Defects	3.7%
282	Myocardial bridging	3.7%
283	Aorticopulmonary Septal Defect	3.7%
284	Hypoalphalipoproteinemias	3.7%
285	Carbamoyl-Phosphate Synthase I Deficiency Disease	3.6%
286	Retrognathia	3.6%
287	Niemann-Pick Disease, Type C	3.6%
288	Multiple Endocrine Neoplasia	3.5%
289	Laryngomalacia	3.5%
290	Truncus Arteriosus, Persistent	3.5%
291	Goldenhar Syndrome	3.5%
292	Pectus carinatum	3.4%
293	Ataxia Telangiectasia	3.4%
294	Bladder Exstrophy	3.4%
295	Congenital Hypothyroidism	3.4%
296	Epispadias	3.4%
297	Familial Periodic Paralysis	3.4%
298	Dermatitis, Atopic	3.4%
299	Multicystic Dysplastic Kidney	3.4%
300	Long QT Syndrome	3.4%
301	Platybasia	3.4%
302	Tricuspid Atresia	3.4%
303	Arrhythmogenic Right Ventricular Dysplasia	3.4%
304	Gonadal Dysgenesis	3.3%
305	Bronchomalacia	3.3%
306	Adrenogenital Syndrome	3.3%
307	Tracheomalacia	3.3%
308	Ovotesticular Disorders of Sex Development	3.3%
309	Lactose Intolerance	3.3%
310	Variegate Porphyria	3.3%
311	Acute intermittent porphyria	3.3%
312	Porphyria Cutanea Tarda	3.3%
313	Hyperhomocysteinemia	3.3%
314	Renal Aminoacidurias	3.3%
315	Fanconi Syndrome	3.3%
316	Pseudohypoaldosteronism	3.3%
317	Liddle Syndrome	3.3%
318	Hyperlipoproteinemia Type IV	3.3%
319	Hyperlipoproteinemia Type V	3.3%
320	Hyperandrogenism	3.2%
321	Prognathism	3.2%
322	Hypokalemic periodic paralysis	3%
323	Mandibulofacial Dysostosis	3%
324	Romano-Ward Syndrome	3%
325	Cystinuria	2.9%
326	Behcet Syndrome	2.9%
327	Talipes	2.8%
328	Gout	2.8%
329	Multiple Endocrine Neoplasia Type 1	2.8%
330	Pseudohypoparathyroidism	2.8%
331	Friedreich Ataxia	2.7%
332	Renal tubular acidosis	2.7%
333	Congenital clubfoot	2.7%
334	Vertical Talus	2.7%
335	Huntington Disease	2.5%
336	Arthritis, Gouty	2.5%
337	Denys-Drash Syndrome	2.4%
338	Familial Hypophosphatemic Rickets	2.2%
339	Nephroblastoma	2.2%
340	Arteriovenous fistula	2.1%
341	Glycosuria, Renal	2%
342	Adenomatous Polyposis Coli	2%
343	MELAS Syndrome	1.6%

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