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==See also==
==See also==
* [[Vitamin D#Synthesis mechanism .28form 3.29]]
* [[Vitamin D#Synthesis mechanism .28form 3.29]]
==Pill Images==
{{TempDrugImages}}
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{{PillImage|fileName=Rocaltrol_NDC_433530633.jpg|drugName=Rocaltrol|NDC=433530633|drugAuthor=Aphena Pharma Solutions - Tennessee, Inc.|ingredients=CALCITRIOL[CALCITRIOL]|pillImprint=R25|dosageValue=0.25|dosageUnit=ug|pillColor=Orange|pillShape=Oval|pillSize=10|pillScore=1}}
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{{PillImage|fileName=CALCITRIOL_NDC_633040240.jpg|drugName=CALCITRIOL|NDC=633040240|drugAuthor=Ranbaxy Pharmaceuticals Inc.|ingredients=CALCITRIOL[CALCITRIOL]|pillImprint=R50|dosageValue=0.5|dosageUnit=ug|pillColor=Orange|pillShape=Oval|pillSize=12|pillScore=1}}
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{{PillImage|fileName=Calcitriol_NDC_00930658.jpg|drugName=Calcitriol|NDC=00930658|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=CALCITRIOL[CALCITRIOL]|pillImprint=93;658|dosageValue=0.5|dosageUnit=ug|pillColor=Brown;Pink|pillShape=Oval|pillSize=13|pillScore=1}}
{{PillImage|fileName=Calcitriol_NDC_00540007.jpg|drugName=Calcitriol|NDC=00540007|drugAuthor=Roxane Laboratories, Inc.|ingredients=CALCITRIOL[CALCITRIOL]|pillImprint=547|dosageValue=0.25|dosageUnit=ug|pillColor=Yellow|pillShape=Oval|pillSize=16|pillScore=1}}


==Additional images==
==Additional images==

Revision as of 20:20, 17 July 2014

Calcitriol (oral)
Clinical data
Pregnancy
category
Routes of
administration
Oral, IV, topical
ATC code
Legal status
Legal status
  • S4 (Au), POM (UK)
Pharmacokinetic data
MetabolismRenal
Elimination half-life5–8 hours
ExcretionRenal
Identifiers
CAS Number
PubChem CID
DrugBank
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaC27H44O3
Molar mass416.64 g/mol

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]


For patient information, click here

Overview

Calcitriol (INN) (Template:PronEng) or 1,25-dihydroxycholecalciferol (abbreviated 1,25-(OH)2D3) is the active form of vitamin D found in the body (vitamin D3). It increases the absorption of calcium and phosphate from the gastrointestinal tract and kidneys and inhibits release of PTH.

Calcitriol is marketed under various trade names including Rocaltrol (Roche), Calcijex (Abbott) and Decostriol (Mibe, Jesalis).

Production and function

It is produced in the kidneys via 25-Hydroxyvitamin D3 1-alpha-Hydroxylase by conversion from 25-hydroxycholecalciferol (calcidiol).

This is stimulated by a decrease in serum calcium and/or phosphate (PO43−), and an increase in parathyroid hormone (PTH) levels. It increases blood calcium levels by increasing the absorption of calcium and phosphate from the gastrointestinal tract, increasing calcium and phosphate reabsorption in the kidneys and inhibiting the release of PTH.

Calcitriol is also commonly used as a medication in the treatment of hypocalcemia and osteoporosis.

Metabolism

Calcitriol becomes calcitroic acid through the action of 24-hydroxylase. Calcitroic acid is excreted in the urine.

Indications

Calcitriol is indicated for:[1]

Calcitriol is also sometimes used topically in the treatment of psoriasis, however the evidence to support its efficacy is inconclusive.[2] The vitamin D analogue calcipotriol is more commonly used for psoriasis.

Adverse effects

The main adverse drug reaction associated with calcitriol therapy is hypercalcaemia – early symptoms include: nausea, vomiting, constipation, anorexia, apathy, headache, thirst, sweating, and/or polyuria). Compared to other vitamin D compounds in clinical use (cholecalciferol, ergocalciferol), calcitriol has a higher risk of inducing hypercalcaemia. However, such episodes may be shorter and easier to treat due to its relatively short half-life.[1]

See also

Pill Images

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Additional images

References

  1. 1.0 1.1 Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006. ISBN 0-9757919-2-3
  2. Calcitriol. In: Klasco RK, editor. Drugdex system. vol 128. Greenwood Village (CO): Thomson Micromedex; 2006.


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