Stem definition | Drug id | CAS RN |
---|---|---|
4250 | 21645-51-2 |
Dose | Unit | Route |
---|---|---|
5 | g | O |
None
Date | Agency | Company | Orphan |
---|---|---|---|
Dec. 9, 1983 | FDA | SANOFI AVENTIS US |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Schizoaffective disorder | 529.01 | 19.53 | 103 | 3929 | 3459 | 63481531 |
Drug level increased | 343.57 | 19.53 | 104 | 3928 | 22632 | 63462358 |
Electrocardiogram QT prolonged | 259.18 | 19.53 | 108 | 3924 | 59422 | 63425568 |
Drug interaction | 166.48 | 19.53 | 128 | 3904 | 229003 | 63255987 |
Sinus rhythm | 42.21 | 19.53 | 10 | 4022 | 846 | 63484144 |
Delirium | 35.94 | 19.53 | 28 | 4004 | 50513 | 63434477 |
Acute myocardial infarction | 27.74 | 19.53 | 20 | 4012 | 32104 | 63452886 |
Drug ineffective | 25.16 | 19.53 | 18 | 4014 | 1044747 | 62440243 |
Hyponatraemia | 24.86 | 19.53 | 33 | 3999 | 111867 | 63373123 |
Coma scale abnormal | 24.54 | 19.53 | 10 | 4022 | 5143 | 63479847 |
Maternal drugs affecting foetus | 24.37 | 19.53 | 10 | 4022 | 5232 | 63479758 |
Morbid thoughts | 24.17 | 19.53 | 6 | 4026 | 617 | 63484373 |
Hypercapnia | 24.03 | 19.53 | 10 | 4022 | 5421 | 63479569 |
Acute kidney injury | 23.86 | 19.53 | 52 | 3980 | 263363 | 63221627 |
Erysipelas | 23.47 | 19.53 | 11 | 4021 | 7894 | 63477096 |
Periventricular leukomalacia | 20.71 | 19.53 | 4 | 4028 | 127 | 63484863 |
Agitation | 20.50 | 19.53 | 22 | 4010 | 59735 | 63425255 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Mesothelioma | 46.38 | 19.33 | 10 | 2803 | 435 | 34953683 |
Violence-related symptom | 23.66 | 19.33 | 6 | 2807 | 530 | 34953588 |
IVth nerve paresis | 19.91 | 19.33 | 3 | 2810 | 15 | 34954103 |
Exposure during pregnancy | 19.75 | 19.33 | 11 | 2802 | 8923 | 34945195 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Acute myocardial infarction | 40.58 | 17.04 | 36 | 5070 | 77000 | 79662282 |
Violence-related symptom | 33.18 | 17.04 | 8 | 5098 | 723 | 79738559 |
Hyponatraemia | 26.97 | 17.04 | 44 | 5062 | 177804 | 79561478 |
General physical health deterioration | 24.22 | 17.04 | 54 | 5052 | 275184 | 79464098 |
Morbid thoughts | 22.62 | 17.04 | 6 | 5100 | 796 | 79738486 |
Hypercapnia | 22.10 | 17.04 | 11 | 5095 | 8924 | 79730358 |
Mesothelioma | 21.87 | 17.04 | 5 | 5101 | 359 | 79738923 |
Drug ineffective | 21.08 | 17.04 | 23 | 5083 | 1080890 | 78658392 |
Cardio-respiratory arrest | 20.88 | 17.04 | 30 | 5076 | 108480 | 79630802 |
Blood phosphorus increased | 20.58 | 17.04 | 11 | 5095 | 10336 | 79728946 |
Erysipelas | 20.09 | 17.04 | 11 | 5095 | 10839 | 79728443 |
Appendicolith | 19.61 | 17.04 | 10 | 5096 | 8541 | 79730741 |
Coma scale abnormal | 19.47 | 17.04 | 10 | 5096 | 8668 | 79730614 |
Cerebrovascular accident | 19.05 | 17.04 | 35 | 5071 | 155257 | 79584025 |
Vomiting | 18.61 | 17.04 | 88 | 5018 | 665740 | 79073542 |
Acute kidney injury | 18.61 | 17.04 | 74 | 5032 | 519330 | 79219952 |
Myeloid maturation arrest | 17.78 | 17.04 | 3 | 5103 | 43 | 79739239 |
Seizure | 17.67 | 17.04 | 38 | 5068 | 188796 | 79550486 |
Anal incontinence | 17.18 | 17.04 | 12 | 5094 | 18156 | 79721126 |
Diabetic foot | 17.07 | 17.04 | 7 | 5099 | 3625 | 79735657 |
None
Source | Code | Description |
---|---|---|
ATC | A02AB01 | ALIMENTARY TRACT AND METABOLISM DRUGS FOR ACID RELATED DISORDERS ANTACIDS Aluminium compounds |
ATC | A02AB02 | ALIMENTARY TRACT AND METABOLISM DRUGS FOR ACID RELATED DISORDERS ANTACIDS Aluminium compounds |
MeSH PA | D000276 | Adjuvants, Immunologic |
MeSH PA | D000863 | Antacids |
MeSH PA | D005765 | Gastrointestinal Agents |
MeSH PA | D007155 | Immunologic Factors |
CHEBI has role | CHEBI:65265 | antacids |
CHEBI has role | CHEBI:79314 | flame retardants |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Peptic ulcer | indication | 13200003 | DOID:750 |
Heartburn | indication | 16331000 | |
Duodenal ulcer disease | indication | 51868009 | DOID:1724 |
Indigestion | indication | 162031009 | |
Gastroesophageal reflux disease | indication | 235595009 | DOID:8534 |
Gastric ulcer | indication | 397825006 | DOID:10808 |
Gastric Hypersecretory Conditions | indication |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 4.51 | acidic |
pKa2 | 4.99 | acidic |
pKa3 | 5.47 | acidic |
None
None
None
ID | Source |
---|---|
4018607 | VUID |
N0000146920 | NUI |
D02807 | KEGG_DRUG |
4017984 | VANDF |
4018607 | VANDF |
4019302 | VANDF |
C0002371 | UMLSCUI |
CHEBI:33130 | CHEBI |
CHEMBL3833310 | ChEMBL_ID |
CHEMBL1200706 | ChEMBL_ID |
D000536 | MESH_DESCRIPTOR_UI |
1945 | INN_ID |
03J11K103C | UNII |
DB06723 | DRUGBANK_ID |
612 | RXNORM |
4159 | MMSL |
5582 | MMSL |
7537 | MMSL |
d00978 | MMSL |
001123 | NDDF |
007943 | NDDF |
273944007 | SNOMEDCT_US |
725733004 | SNOMEDCT_US |
768557001 | SNOMEDCT_US |
80399002 | SNOMEDCT_US |
1330-44-5 | SECONDARY_CAS_RN |
6328660 | PUBCHEM_CID |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
Good Sense antacid | HUMAN OTC DRUG LABEL | 3 | 0113-0340 | SUSPENSION | 800 mg | ORAL | OTC monograph final | 13 sections |
Good Sense AntacidRegular Strength | HUMAN OTC DRUG LABEL | 3 | 0113-0357 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 13 sections |
Good Sense AntacidMaximum Strength | HUMAN OTC DRUG LABEL | 3 | 0113-0588 | SUSPENSION | 800 mg | ORAL | OTC monograph final | 13 sections |
good sense antacid | HUMAN OTC DRUG LABEL | 3 | 0113-0851 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 13 sections |
Mag-AL Liquid | HUMAN OTC DRUG LABEL | 2 | 0121-1760 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 14 sections |
Mag-AL Liquid | HUMAN OTC DRUG LABEL | 2 | 0121-1760 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 14 sections |
Mag-AL Plus | HUMAN OTC DRUG LABEL | 3 | 0121-1761 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 14 sections |
Mag-AL Plus | HUMAN OTC DRUG LABEL | 3 | 0121-1761 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 14 sections |
Mag-AL Plus | HUMAN OTC DRUG LABEL | 3 | 0121-1761 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 14 sections |
Mag-AL PlusXS | HUMAN OTC DRUG LABEL | 3 | 0121-1762 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 15 sections |
Mag-AL PlusXS | HUMAN OTC DRUG LABEL | 3 | 0121-1762 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 15 sections |
GAVISCON | HUMAN OTC DRUG LABEL | 2 | 0135-0094 | LIQUID | 95 mg | ORAL | OTC monograph final | 13 sections |
GAVISCON | HUMAN OTC DRUG LABEL | 2 | 0135-0095 | LIQUID | 254 mg | ORAL | OTC monograph final | 13 sections |
GavisconRegular Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0096 | TABLET, CHEWABLE | 80 mg | ORAL | NDA | 15 sections |
GavisconRegular Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0096 | TABLET, CHEWABLE | 80 mg | ORAL | NDA | 15 sections |
GavisconExtra Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0098 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 15 sections |
GavisconExtra Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0098 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 15 sections |
GavisconExtra Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0430 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 15 sections |
GavisconExtra Strength | HUMAN OTC DRUG LABEL | 2 | 0135-0430 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 15 sections |
GAVISCON | HUMAN OTC DRUG LABEL | 2 | 0135-0574 | LIQUID | 254 mg | ORAL | OTC monograph final | 13 sections |
Antacid Mint | HUMAN OTC DRUG LABEL | 3 | 0363-0432 | SUSPENSION | 200 mg | ORAL | OTC MONOGRAPH FINAL | 14 sections |
Antacid Mint | HUMAN OTC DRUG LABEL | 3 | 0363-0432 | SUSPENSION | 200 mg | ORAL | OTC MONOGRAPH FINAL | 14 sections |
Antacid Mint | HUMAN OTC DRUG LABEL | 3 | 0363-0432 | SUSPENSION | 200 mg | ORAL | OTC MONOGRAPH FINAL | 14 sections |
Antacid antigasMaximum Strength | HUMAN OTC DRUG LABEL | 3 | 0363-0528 | LIQUID | 800 mg | ORAL | OTC MONOGRAPH FINAL | 15 sections |
FAST ACTING Heartburn Relief | HUMAN OTC DRUG LABEL | 2 | 0363-1155 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 12 sections |
FAST ACTING Heartburn Relief | HUMAN OTC DRUG LABEL | 2 | 0363-1155 | TABLET, CHEWABLE | 160 mg | ORAL | OTC monograph final | 12 sections |
ADVANCED REGULAR STRENGTH ANTACID | HUMAN OTC DRUG LABEL | 3 | 0363-1639 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 10 sections |
ADVANCED REGULAR STRENGTH ANTACID | HUMAN OTC DRUG LABEL | 3 | 0363-1639 | SUSPENSION | 200 mg | ORAL | OTC monograph final | 10 sections |
MAXIMUM STRENGTH ANTACID ANTIGAS | HUMAN OTC DRUG LABEL | 3 | 0363-1691 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 10 sections |
MAXIMUM STRENGTH ANTACID ANTIGAS | HUMAN OTC DRUG LABEL | 3 | 0363-1691 | SUSPENSION | 400 mg | ORAL | OTC monograph final | 10 sections |