colestipol 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
728 50925-79-6

Description:

MoleculeDescription

Synonyms:

  • colestipol
  • cholestabyl
  • cholestipol
  • colestipol hydrochloride
  • colestipol HCl
Highly crosslinked and insoluble basic anion exchange resin used as anticholesteremic. It may also may reduce triglyceride levels.
  • Molecular weight:
  • Formula:
  • CLOGP:
  • LIPINSKI: None
  • HAC: None
  • HDO: None
  • TPSA:
  • ALOGS:
  • ROTB: None

Drug dosage:

DoseUnitRoute
20 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 4 Bocci G, Oprea TI, Benet LZ

Approvals:

DateAgencyCompanyOrphan
April 4, 1977 FDA PHARMACIA AND UPJOHN

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Diarrhoea 111.95 21.12 191 4414 715175 62769242
Product physical issue 85.62 21.12 26 4579 4954 63479463
Fistula 43.10 21.12 19 4586 10374 63474043
Mucous stools 35.98 21.12 13 4592 4235 63480182
Vaginal abscess 35.97 21.12 8 4597 447 63483970
Product dose omission issue 35.46 21.12 62 4543 234251 63250166
Anal skin tags 34.86 21.12 8 4597 515 63483902
Infusion site streaking 34.83 21.12 8 4597 517 63483900
Clostridium difficile infection 33.51 21.12 23 4582 29899 63454518
Rectal fissure 32.89 21.12 8 4597 662 63483755
Intestinal obstruction 32.84 21.12 23 4582 30876 63453541
Vitamin D increased 32.40 21.12 8 4597 704 63483713
Feeding intolerance 31.74 21.12 8 4597 766 63483651
Procedural anxiety 31.72 21.12 8 4597 768 63483649
Product use complaint 30.40 21.12 10 4595 2464 63481953
Frequent bowel movements 28.91 21.12 19 4586 23003 63461414
Lactose intolerance 28.58 21.12 10 4595 2968 63481449
Cholangitis sclerosing 25.79 21.12 8 4597 1633 63482784
Haemorrhoids 24.74 21.12 17 4588 22133 63462284
Poor quality product administered 24.28 21.12 9 4596 3147 63481270
Flatulence 24.00 21.12 20 4585 34682 63449735
Gastrointestinal ulcer 23.57 21.12 8 4597 2167 63482250
Haematocrit increased 23.05 21.12 8 4597 2318 63482099
White blood cell disorder 22.38 21.12 8 4597 2526 63481891
Anorectal discomfort 22.06 21.12 8 4597 2631 63481786
Gingival swelling 21.35 21.12 9 4596 4409 63480008

FDA Adverse Event Reporting System (Male)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Diarrhoea 63.10 23.76 75 1248 389837 34565771
Intestinal stenosis 24.17 23.76 7 1316 2179 34953429

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Diarrhoea 86.38 20.05 167 4345 880322 78859554
Fistula 53.64 20.05 22 4490 12918 79726958
Product physical issue 51.68 20.05 16 4496 4169 79735707
Vaginal abscess 38.74 20.05 8 4504 404 79739472
Anal skin tags 37.57 20.05 8 4504 469 79739407
Rectal fissure 36.92 20.05 9 4503 966 79738910
Infusion site streaking 36.76 20.05 8 4504 520 79739356
Mucous stools 36.65 20.05 13 4499 5149 79734727
Vitamin D increased 35.52 20.05 8 4504 609 79739267
Procedural anxiety 33.80 20.05 8 4504 758 79739118
Intestinal obstruction 33.41 20.05 24 4488 42996 79696880
Feeding intolerance 32.87 20.05 8 4504 852 79739024
Lactose intolerance 29.15 20.05 9 4503 2321 79737555
Clostridium difficile infection 29.06 20.05 22 4490 42663 79697213
Intestinal resection 28.73 20.05 10 4502 3747 79736129
Product use complaint 28.59 20.05 9 4503 2474 79737402
Cholangitis sclerosing 28.06 20.05 9 4503 2628 79737248
Frequent bowel movements 26.48 20.05 18 4494 29521 79710355
Large intestinal ulcer 26.35 20.05 10 4502 4787 79735089
Intestinal stenosis 24.94 20.05 9 4503 3745 79736131
COVID-19 23.23 20.05 36 4476 157638 79582238
Gingival swelling 23.14 20.05 9 4503 4600 79735276
Product dose omission issue 22.82 20.05 46 4466 247491 79492385
White blood cell disorder 22.51 20.05 8 4504 3184 79736692
Haemorrhoids 22.04 20.05 16 4496 29112 79710764
Gastrointestinal ulcer 21.92 20.05 8 4504 3438 79736438
Anorectal discomfort 21.55 20.05 8 4504 3603 79736273
Cystic fibrosis 20.99 20.05 8 4504 3872 79736004
Female genital tract fistula 20.88 20.05 9 4503 5966 79733910
Diverticulum 20.73 20.05 12 4500 14884 79724992
Haematocrit increased 20.69 20.05 8 4504 4026 79735850
Flatulence 20.58 20.05 18 4494 42706 79697170
Oesophageal pain 20.23 20.05 8 4504 4271 79735605

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC C10AC02 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, PLAIN
Bile acid sequestrants
FDA MoA N0000175365 Bile-acid Binding Activity
CHEBI has role CHEBI:35821 anticholesteremic drugs
MeSH PA D000837 Anion Exchange Resins
MeSH PA D000963 Antimetabolites
MeSH PA D000960 Hypolipidemic Agents
MeSH PA D007475 Ion Exchange Resins
MeSH PA D057847 Lipid Regulating Agents
MeSH PA D064449 Sequestering Agents
FDA EPC N0000180292 Bile Acid Sequestrant

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Hypercholesterolemia indication 13644009
Hyperlipidemia indication 55822004 DOID:1168
Poisoning by digitalis glycoside off-label use 12876009
Biliary Obstruction with Pruritus off-label use
Constipation contraindication 14760008 DOID:2089
Blood coagulation disorder contraindication 64779008 DOID:1247
Hemorrhoids contraindication 70153002 DOID:9746
Kidney disease contraindication 90708001 DOID:557
Calculus in biliary tract contraindication 266474003
Complete Biliary Obstruction contraindication




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
4019692 VUID
N0000147784 NUI
D02113 KEGG_DRUG
37296-80-3 SECONDARY_CAS_RN
104485 RXNORM
4018086 VANDF
4019692 VANDF
C0009279 UMLSCUI
CHEBI:3814 CHEBI
CHEMBL1909303 ChEMBL_ID
CHEMBL1201474 ChEMBL_ID
DB00375 DRUGBANK_ID
D003084 MESH_DESCRIPTOR_UI
62816 PUBCHEM_CID
2738 INN_ID
K50N755924 UNII
4494 MMSL
83640 MMSL
d00744 MMSL
001217 NDDF
004708 NDDF
372811005 SNOMEDCT_US
55316001 SNOMEDCT_US
66971004 SNOMEDCT_US
26658-42-4 SECONDARY_CAS_RN

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0260 GRANULE, FOR SUSPENSION 5 g ORAL NDA 18 sections
Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0260 GRANULE, FOR SUSPENSION 5 g ORAL NDA 18 sections
Flavored Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0370 GRANULE, FOR SUSPENSION 5 g ORAL NDA 18 sections
Flavored Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0370 GRANULE, FOR SUSPENSION 5 g ORAL NDA 18 sections
Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0450 TABLET 1 g ORAL NDA 18 sections
Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0450 TABLET 1 g ORAL NDA 18 sections
Colestid HUMAN PRESCRIPTION DRUG LABEL 1 0009-0450 TABLET 1 g ORAL NDA 18 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-2142 TABLET, FILM COATED 1 g ORAL ANDA 20 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-2142 TABLET, FILM COATED 1 g ORAL ANDA 20 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5211 TABLET, FILM COATED 1 g ORAL ANDA 20 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5211 TABLET, FILM COATED 1 g ORAL ANDA 20 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5212 SUSPENSION 5 g ORAL ANDA 14 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5212 SUSPENSION 5 g ORAL ANDA 14 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5213 SUSPENSION 5 g ORAL ANDA 14 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 0115-5213 SUSPENSION 5 g ORAL ANDA 14 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 54868-0610 TABLET 1 g ORAL NDA authorized generic 19 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 59762-0260 GRANULE, FOR SUSPENSION 5 g ORAL NDA AUTHORIZED GENERIC 19 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 59762-0260 GRANULE, FOR SUSPENSION 5 g ORAL NDA AUTHORIZED GENERIC 19 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 59762-0450 TABLET 1 g ORAL NDA AUTHORIZED GENERIC 19 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 59762-0450 TABLET 1 g ORAL NDA AUTHORIZED GENERIC 19 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 60687-715 TABLET, FILM COATED 1 g ORAL ANDA 19 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 62559-395 TABLET, FILM COATED 1 g ORAL ANDA 16 sections
Colestipol Hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 68151-4361 TABLET 1 g ORAL NDA AUTHORIZED GENERIC 18 sections
COLESTIPOL HYDROCHLORIDE HUMAN PRESCRIPTION DRUG LABEL 1 70518-2693 TABLET, FILM COATED 1 g ORAL ANDA 19 sections
Colestipol hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 70710-1467 TABLET, FILM COATED 1 g ORAL ANDA 16 sections
Colestipol hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 70771-1653 TABLET, FILM COATED 1 g ORAL ANDA 1 sections
Colestipol hydrochloride HUMAN PRESCRIPTION DRUG LABEL 1 70771-1653 TABLET, FILM COATED 1 g ORAL ANDA 1 sections