| 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 |