Hectorol
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Hectorol
SIDE EFFECTS
Dialysis
Hectorol (doxercalciferol liquid filled capsule) has been evaluated for safety in clinical studies in 165 patients with chronic kidney disease on hemodialysis. In two placebo-controlled, double-blind, multicenter studies, discontinuation of therapy due to any adverse event occurred in 2.9% of 138 patients treated with Hectorol (doxercalciferol liquid filled capsule) for four to six months (dosage titrated to achieve target iPTH levels, see CLINICAL PHARMACOLOGY/Clinical Studies) and in 3.3% of 61 patients treated with placebo for two months. Adverse events occurring in the Hectorol (doxercalciferol liquid filled capsule) group at a frequency of 2% or greater and more frequently than in the placebo group are presented in Table 3 below:
Table 3: Adverse Events Reported by ≥ 2% of Hectorol® (doxercalciferol liquid filled capsule) Treated
Patients and More Frequently Than Placebo During the Double-blind Phase of Two
Clinical Studies
| Adverse Event | Hectorol® (n=61) % |
Placebo (n=61) % |
| Body as a Whole | ||
| Abscess | 3.3 | 0.0 |
| Headache | 27.9 | 18.0 |
| Malaise | 27.9 | 19.7 |
| Cardiovascular System | ||
| Bradycardia | 6.6 | 4.9 |
| Digestive System | ||
| Anorexia | 4.9 | 3.3 |
| Constipation | 3.3 | 3.3 |
| Dyspepsia | 4.9 | 1.6 |
| Nausea/Vomiting | 21.3 | 19.7 |
| Musculoskeletal System | ||
| Arthralgia | 4.9 | 0.0 |
| Metabolic and Nutritional | ||
| Edema | 34.4 | 21.3 |
| Weight increase | 4.9 | 0.0 |
| Nervous System | ||
| Dizziness | 11.5 | 9.8 |
| Sleep disorder | 3.3 | 0.0 |
| Respiratory System | ||
| Dyspnea | 11.5 | 6.6 |
| Skin | ||
| Pruritus | 8.2 | 6.6 |
| A patient who reported the same medical term more than once was counted only once for that medical term. | ||
Pre-dialysis
Hectorol (doxercalciferol liquid filled capsule) has been evaluated for safety in clinical studies in 55 patients (27 active and 28 placebo) with chronic kidney disease, Stages 3 or 4. In two placebo-controlled, double-blind, multicenter studies, discontinuation of therapy due to any adverse event occurred in one (3.7%) of 27 patients treated with Hectorol (doxercalciferol liquid filled capsule) for 24 weeks (dosage titrated to achieve target iPTH levels, see CLINICAL PHARMACOLOGY/Clinical Studies) and in three (10.7%) of 28 patients treated with placebo for 24 weeks. Adverse events occurring in the Hectorol (doxercalciferol liquid filled capsule) group at a frequency of 5% or greater and more frequently than in the placebo group are as follows: Body as a Whole - Infection, Chest Pain; Digestive System - Constipation, Dyspepsia; Hematologic and Lymphatic - Anemia; Metabolic and Nutritional - Dehydration; Nervous System - Depression, Hypertonia, Insomnia, Paresthesia; Respiratory System - Cough increased, Dyspnea, Rhinitis.
Potential adverse effects of Hectorol (doxercalciferol liquid filled capsule) are, in general, similar to those encountered with excessive vitamin D intake. The early and late signs and symptoms of vitamin D intoxication associated with hypercalcemia include:
Early
Weakness, headache, somnolence, nausea, vomiting, dry mouth, constipation, muscle pain, bone pain, metallic taste, and anorexia.
Late
Polyuria, polydipsia, anorexia, weight loss, nocturia, conjunctivitis (calcific), pancreatitis, photophobia, rhinorrhea, pruritus, hyperthermia, decreased libido, elevated blood urea nitrogen (BUN), albuminuria, hypercholesterolemia, elevated serum aspartate transaminase (AST) and alanine transaminase (ALT), ectopic calcification, hypertension, cardiac arrhythmias, sensory disturbances, dehydration, apathy, arrested growth, urinary tract infections, and, rarely, overt psychosis.
Read the Hectorol (doxercalciferol liquid filled capsule) Side Effects Center for a complete guide to possible side effects »
DRUG INTERACTIONS
Specific drug interaction studies have not been conducted. Cholestyramine has been reported to reduce intestinal absorption of fat-soluble vitamins; therefore, it may impair intestinal absorption of doxercalciferol. Magnesium-containing antacids and Hectorol (doxercalciferol liquid filled capsule) should not be used concomitantly because such use may lead to the development of hypermagnesemia (see WARNINGS). The use of mineral oil or other substances that may affect absorption of fat may influence the absorption and availability of Hectorol (doxercalciferol liquid filled capsule) . Although not examined specifically, enzyme inducers (such as glutethimide and phenobarbital) may affect the 25-hydroxylation of Hectorol (doxercalciferol liquid filled capsule) and may necessitate dosage adjustments. Cytochrome P450 inhibitors (such as ketoconazole and erythromycin) may inhibit the 25-hydroxylation of Hectorol (doxercalciferol liquid filled capsule) . Hence, formation of the active Hectorol (doxercalciferol liquid filled capsule) moiety may be hindered.
Last reviewed on RxList: 4/12/2011
This monograph has been modified to include the generic and brand name in many instances.
Additional Hectorol Information
Hectorol - User Reviews
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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