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Calcitriol

A11C - Vitamin A and D, incl. combinations ATC A11CC04 Small molecule approved 1978 Oral Parenteral Topical Natural product

JFDA label: ROCALTROL CAP

Mechanism of Action

Agonist of Vitamin D3 receptor — Vitamin D receptor agonist

TargetActionGene / class
Vitamin D3 receptor efficacy AGONIST VDR

Indications

Approved

  • Hypocalcemia — Hypocalcemia
  • Hypoparathyroidism — hypoparathyroidism
  • Kidney Failure, Chronic — chronic kidney disease
  • Psoriasis — psoriasis

Off-label

  • Acute Kidney Injury
  • Adenomatous Polyposis Coli
  • Breast Neoplasms
  • Carcinoma, Basal Cell
  • Cholangiocarcinoma
  • Chronic Kidney Disease-Mineral and Bone Disorder
  • Diabetes Mellitus, Type 1
  • Diabetic Nephropathies
  • Fibroma
  • Hyperparathyroidism, Secondary
  • Hypertension
  • Klinefelter Syndrome
  • Lupus Erythematosus, Systemic
  • Myelodysplastic Syndromes
  • Osteopetrosis
  • Osteoporosis
  • Pancreatic Neoplasms
  • Prostatic Neoplasms
  • Prostatic Neoplasms, Castration-Resistant
  • Sepsis
  • Severe Acute Respiratory Syndrome

Contraindications

Source: openFDA

  • Calcitriol Oral Solution should not be given to patients with hypercalcemia or evidence of vitamin D toxicity. Use of Calcitriol Oral Solution in patients with known hypersensitivity to Calcitriol Oral Solution (or drugs of the same class) or any of the inactive ingredients is contraindicated. Absolute

Adverse Reactions

Very Common >10%Common 1–10%Uncommon 0.1–1% Rare 0.01–0.1%Very Rare <0.01%Not Known

Nervous system disorders (2)

Not Known Headache · Somnolence

Metabolism and nutrition disorders (1)

Not Known Weight Loss

Gastrointestinal disorders (8)

Not Known Abdominal Pain Or Stomach Ache Late Polyuria · And Anorexia · Anorexia · Constipation · Dry Mouth · Nausea · Pancreatitis · Vomiting

Skin and subcutaneous tissue disorders (1)

Not Known Pruritus

Musculoskeletal and connective tissue disorders (1)

Not Known Bone Pain

Eye disorders (2)

Not Known Conjunctivitis Calcific · Photophobia

General disorders and administration site conditions (5)

Not Known Metallic Taste · Muscle Pain · Nocturia · Polydipsia · Weakness

Respiratory, thoracic and mediastinal disorders (1)

Not Known Rhinorrhea

Dosing

Source: openFDA

The optimal daily dose of Calcitriol Oral Solution must be carefully determined for each patient. Calcitriol Oral Solution can be administered as an oral solution (1 mcg/mL). Calcitriol Oral Solution therapy should always be started at the lowest possible dose and should not be increased without careful monitoring of serum calcium. The effectiveness of Calcitriol Oral Solution therapy is predicated on the assumption that each patient is receiving an adequate but not excessive daily intake of calcium. Patients are advised to have a dietary intake of calcium at a minimum of 600 mg daily. The U.S. RDA for calcium in adults is 800 mg to 1200 mg. To ensure that each patient receives an adequate daily intake of calcium, the physician should either prescribe a calcium supplement or instruct the patient in proper dietary measures. Because of improved calcium absorption from the gastrointestinal tract, some patients on Calcitriol Oral Solution may be maintained on a lower calcium intake. Patients who tend to develop hypercalcemia may require only low doses of calcium or no supplementation at all. During the titration period of treatment with Calcitriol Oral Solution, serum calcium levels should be checked at least twice weekly. When the optimal dosage of Calcitriol Oral Solution has been determined, serum calcium levels should be checked every month (or as given below for individual indications). Samples for serum calcium estimation should be taken without a tourniquet. Dialysis Patients The recommended initial dose of Calcitriol Oral Solution is 0.25 mcg/day. If a satisfactory response in the biochemical parameters and clinical manifestations of the disease state is not observed, dosage may be increased by 0.25 mcg/day at 4- to 8-week intervals. During this titration period, serum calcium levels should be obtained at least twice weekly, and if hypercalcemia is noted, the drug should be immediately discontinued until normocalcemia ensues (see PRECAUTIONS: GENERAL ). Phosphorus, magnesium, and alkaline phosphatase should be determined periodically. Patients with normal or only slightly reduced serum calcium levels may respond to Calcitriol Oral Solution doses of 0.25 mcg every other day. Most patients undergoing hemodialysis respond to doses between 0.5 and 1 mcg/day. Calcitriol Oral Solution may normalize plasma-ionized calcium in some uremic patients, yet fail to suppress parathyroid hyperfunction. In these individuals with autonomous parathyroid hyper-function, Calcitriol Oral Solution may be useful to maintain normocalcemia, but has not been shown to be adequate treatment for hyperparathyroidism. Hypoparathyroidism The recommended initial dosage of Calcitriol Oral Solution is 0.25 mcg/day given in the morning. If a satisfactory response in the biochemical parameters and clinical manifestations of the disease is not observed, the dose may be increased at 2- to 4-week intervals. During the dosage titration period, serum calcium levels should be obtained at least twice weekly and, if hypercalcemia is noted, Calcitriol Oral Solution should be immediately discontinued until normocalcemia ensues (see PRECAUTIONS: GENERAL ). Careful consideration should also be given to lowering the dietary calcium intake. Serum calcium, phosphorus, and 24-hour urinary calcium should be determined periodically. Most adult patients and pediatric patients age 6 years and older have responded to dosages in the range of 0.5 mcg to 2 mcg daily. Pediatric patients in the 1- to 5-year age group with hypoparathyroidism have usually been given 0.25 mcg to 0.75 mcg daily. The number of treated patients with pseudohypoparathyroidism less than 6 years of age is too small to make dosage recommendations. Malabsorption is occasionally noted in patients with hypoparathyroidism; hence, larger doses of Calcitriol Oral Solution may be needed. Predialysis Patients The recommended initial dosage of Calcitriol Oral Solution is 0.25 mcg/day in adults and pediatric patients 3 yea

Warnings & Precautions

Source: openFDA

Warnings & Precautions

Overdosage of any form of vitamin D is dangerous (see OVERDOSAGE ). Progressive hypercalcemia due to overdosage of vitamin D and its metabolites may be so severe as to require emergency attention. Chronic hypercalcemia can lead to generalized vascular calcification, nephrocalcinosis and other soft-tissue calcification. The serum calcium times phosphate (Ca x P) product should not be allowed to exceed 70 mg 2 /dL 2 . Radiographic evaluation of suspect anatomical regions may be useful in the early detection of this condition. Calcitriol Oral Solution is the most potent metabolite of vitamin D available. The administration of Calcitriol Oral Solution to patients in excess of their daily requirements can cause hypercalcemia, hypercalciuria, and hyperphosphatemia. Therefore, pharmacologic doses of vitamin D and its derivatives should be withheld during Calcitriol Oral Solution treatment to avoid possible additive effects and hypercalcemia. If treatment is switched from ergocalciferol (vitamin D 2 ) to calcitriol, it may take several months for the ergocalciferol level in the blood to return to the baseline value (see OVERDOSAGE ). Calcitriol increases inorganic phosphate levels in serum. While this is desirable in patients with hypophosphatemia, caution is called for in patients with renal failure because of the danger of ectopic calcification. A nonaluminum phosphate-binding compound and a low-phosphate diet should be used to control serum phosphorus levels in patients undergoing dialysis. Magnesium-containing preparations (eg, antacids) and Calcitriol Oral Solution should not be used concomitantly in patients on chronic renal dialysis because such use may lead to the development of hypermagnesemia. Studies in dogs and rats given calcitriol for up to 26 weeks have shown that small increases of calcitriol above endogenous levels can lead to abnormalities of calcium metabolism with the potential for calcification of many tissues in the body.

Pregnancy & Lactation

Pregnancy

Lactation

Compatible Hale L1

If the mother requires calcitriol, it is not a reason to discontinue breastfeeding.

Chemistry & Properties

2D structure
FormulaC27H44O3
Molecular weight416.65 g/mol
IUPAC nametrans-(1R,3S,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
CAS32222-06-3
PubChem CID5280453
InChIKeyGMRQFYUYWCNGIN-NKMMMXOESA-N
logP5.7 (XLogP 5.1)
Polar surface area60.69 Ų
H-bond acceptors / donors3 / 3
Drug-likeness (QED)0.52
Lipinski violations1
SMILESC=C1/C(=C\C=C2/CCC[C@]3(C)[C@@H]([C@H](C)CCCC(C)(C)O)CC[C@@H]23)C[C@@H](O)C[C@@H]1O

Biology & Pharmacokinetics

Pharmacokinetics

BBB penetrantNo

Enzyme interactions

EnzymeRoleDetail
CYP2B6Inhibitor
CYP2C8Inhibitor
CYP3A4Substrate

Transporters

BCRP (Inhibitor)BSEP (Inhibitor)BSEP (Inhibitor)MRP1 (Inhibitor)MRP2 (Inhibitor)MRP3 (Inhibitor)OATP1B1 (Inhibitor)OATP1B3 (Inhibitor)OATP2B1 (Inhibitor)P-gp (Inhibitor)P-gp (Substrate)

Drug–drug interactions (55, DDInter)

Interacting drugSeverityManagement
Burosumab major
Calcifediol major
Cholecalciferol major
Dihydrotachysterol major
Doxercalciferol major
Erdafitinib major
Ergocalciferol major
Paricalcitol major
Aluminum hydroxide moderate
Amobarbital moderate
Bendroflumethiazide moderate
Benzthiazide moderate
Butabarbital moderate
Butalbital moderate
Calcipotriol (topical) moderate
Carbamazepine moderate
Chlorothiazide moderate
Chlorthalidone moderate
Cholestyramine moderate
Colesevelam moderate
Colestipol moderate
Digitoxin moderate
Digoxin moderate
Felbamate moderate
Fosphenytoin moderate
Hydrochlorothiazide moderate
Hydroflumethiazide moderate
Indapamide moderate
Isoniazid moderate
Magnesium carbonate moderate
Magnesium chloride moderate
Magnesium citrate moderate
Magnesium gluconate moderate
Magnesium glycinate moderate
Magnesium hydroxide moderate
Magnesium oxide moderate
Magnesium sulfate moderate
Methylphenobarbital moderate
Metolazone moderate
Mineral oil moderate

Showing 40 of 55.

Registered Products (1)

BrandForm / strengthPackAgentCitizen (JOD)
ROCALTROL CAP Capsule 0.25 mcg 100 cap Shawi & Rushedat Drug Store 17.960