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

Stem definitionDrug idCAS RN
iodine-containing contrast media 1471 87771-40-2

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • ioversol
  • joversol
  • MP-328
  • Molecular weight: 807.12
  • Formula: C18H24I3N3O9
  • CLOGP: -2.73
  • LIPINSKI: 3
  • HAC: 12
  • HDO: 8
  • TPSA: 199.89
  • ALOGS: -2.89
  • ROTB: 12

  • Status: OFP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
Dec. 30, 1988 FDA LIEBEL-FLARSHEIM

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
Urticaria 666.60 59.90 286 3999 129275 50471564
Sneezing 345.53 59.90 100 4185 13944 50586895
Throat irritation 334.27 59.90 117 4168 30122 50570717
Pruritus 295.91 59.90 220 4065 283348 50317491
Throat tightness 197.35 59.90 72 4213 20775 50580064
Dyspnoea 185.46 59.90 228 4057 547380 50053459
Anaphylactic shock 170.12 59.90 64 4221 20091 50580748
Contrast media reaction 151.97 59.90 31 4254 976 50599863
Chest discomfort 138.17 59.90 90 4195 92632 50508207
Erythema 132.74 59.90 105 4180 146309 50454530
Eye pruritus 117.44 59.90 43 4242 12491 50588348
Pharyngeal oedema 115.38 59.90 43 4242 13122 50587717
Laryngeal discomfort 107.84 59.90 19 4266 265 50600574
Laryngeal oedema 89.59 59.90 28 4257 5025 50595814
Air embolism 78.19 59.90 14 4271 215 50600624
Rash 77.76 59.90 135 4150 437336 50163503
Type I hypersensitivity 76.78 59.90 21 4264 2364 50598475
Cough 72.09 59.90 95 4190 241169 50359670
Eye swelling 69.57 59.90 34 4251 20110 50580729
Extravasation 66.18 59.90 18 4267 1984 50598855
Bronchospasm 63.35 59.90 29 4256 14825 50586014
Eyelid oedema 61.87 59.90 25 4260 9441 50591398

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
Urticaria 357.94 45.72 146 2512 54514 29517355
Sneezing 197.56 45.72 51 2607 4363 29567506
Anaphylactic shock 192.52 45.72 64 2594 13272 29558597
Pruritus 180.17 45.72 118 2540 116731 29455138
Nephropathy toxic 176.95 45.72 57 2601 10699 29561170
Contrast media reaction 103.94 45.72 22 2636 783 29571086
Throat irritation 102.54 45.72 36 2622 8749 29563120
Air embolism 99.01 45.72 16 2642 119 29571750
Dyspnoea 84.24 45.72 123 2535 326609 29245260
Throat tightness 78.70 45.72 28 2630 7063 29564806
Erythema 71.50 45.72 57 2601 75549 29496320
Anaphylactic reaction 57.71 45.72 34 2624 27539 29544330
Laryngeal oedema 53.50 45.72 17 2641 3031 29568838
Hypersensitivity 48.05 45.72 39 2619 52864 29519005

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
Urticaria 746.49 45.71 325 5303 146992 64346112
Sneezing 360.35 45.71 106 5522 15145 64477959
Anaphylactic shock 333.94 45.71 118 5510 30210 64462894
Pruritus 333.51 45.71 249 5379 312151 64180953
Throat irritation 255.76 45.71 99 5529 32612 64460492
Contrast media reaction 238.20 45.71 50 5578 1762 64491342
Dyspnoea 171.66 45.71 257 5371 718417 63774687
Erythema 163.55 45.71 133 5495 186937 64306167
Throat tightness 159.51 45.71 64 5564 23096 64470008
Laryngeal oedema 123.23 45.71 39 5589 7074 64486030
Laryngeal discomfort 121.29 45.71 23 5605 476 64492628
Pharyngeal oedema 114.15 45.71 45 5583 15486 64477618
Type I hypersensitivity 107.38 45.71 30 5598 3544 64489560
Air embolism 106.50 45.71 20 5608 392 64492712
Chest discomfort 89.70 45.71 77 5551 116029 64377075
Cyanosis 89.37 45.71 42 5586 22113 64470991
Eye pruritus 83.72 45.71 34 5594 12625 64480479
Extravasation 83.37 45.71 24 5604 3156 64489948
Bronchospasm 75.02 45.71 37 5591 21645 64471459
Rash 71.23 45.71 136 5492 458413 64034691
Eye swelling 68.21 45.71 35 5593 22246 64470858
Eyelid oedema 67.79 45.71 29 5599 12250 64480854
Anaphylactic reaction 64.39 45.71 51 5577 68613 64424491
Cough 60.17 45.71 100 5528 302048 64191056
Hypersensitivity 57.66 45.71 78 5550 196374 64296730
Procedural complication 56.71 45.71 22 5606 7243 64485861
Anaphylactoid reaction 54.17 45.71 19 5609 4719 64488385
Blood pressure decreased 52.40 45.71 50 5578 86149 64406955
Shock 50.69 45.71 35 5593 38205 64454899
Loss of consciousness 49.86 45.71 63 5565 148302 64344802
Flushing 46.62 45.71 45 5583 78603 64414501

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC V08AB07 VARIOUS
CONTRAST MEDIA
X-RAY CONTRAST MEDIA, IODINATED
Watersoluble, nephrotropic, low osmolar X-ray contrast media
FDA MoA N0000010258 X-Ray Contrast Activity
MeSH PA D003287 Contrast Media
MeSH PA D064907 Diagnostic Uses of Chemicals
FDA EPC N0000180185 Radiographic Contrast Agent

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

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 10.63 acidic
pKa2 11.03 acidic
pKa3 11.71 acidic
pKa4 13.6 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
4020983 VUID
N0000148454 NUI
D01555 KEGG_DRUG
4020983 VANDF
C0063828 UMLSCUI
CHEBI:31717 CHEBI
CHEMBL1200614 ChEMBL_ID
DB09134 DRUGBANK_ID
C054871 MESH_SUPPLEMENTAL_RECORD_UI
6007 INN_ID
N3RIB7X24K UNII
3741 PUBCHEM_CID
27792 RXNORM
4909 MMSL
d01469 MMSL
003499 NDDF
109222009 SNOMEDCT_US
395759000 SNOMEDCT_US

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray320 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1323 INJECTION 678 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray300 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1332 INJECTION 636 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections
Optiray350 HUMAN PRESCRIPTION DRUG LABEL 1 0019-1333 INJECTION 741 mg INTRA-ARTERIAL NDA 28 sections