Buy Generic Alfacip Online
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Generic Alfacip 0.25mg
Package | Price | Per Cap | Shipping | Order | |
0.25mg x 30 caps | $45.63 | $1.52 | Add to Cart | ||
0.25mg x 60 caps | $65.27 | $1.09 | Add to Cart | ||
0.25mg x 90 caps | $77.92 | $0.87 | Add to Cart | ||
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Generic Alfacip 0.5mg
Package | Price | Per Cap | Shipping | Order | |
0.5mg x 30 caps | $48.79 | $1.63 | Add to Cart | ||
0.5mg x 60 caps | $69.93 | $1.17 | Add to Cart | ||
0.5mg x 90 caps | $93.91 | $1.04 | Add to Cart | ||
0.5mg x 120 caps | $114.55 | $0.95 | Add to Cart | ||
0.5mg x 180 caps | $155.84 | $0.87 | Add to Cart |
Generic Alfacip Information
Introduction
Alfacip is a pharmaceutical product that contains the active compound alfacalcidol, a synthetic analogue of vitamin D₃. It belongs to the general health medication group and is primarily prescribed for the management of disorders associated with impaired calcium and bone metabolism. In the United Kingdom, Alfacip is used to maintain adequate serum calcium levels in patients at risk of deficiency, thereby supporting skeletal health and reducing the clinical sequ‑itude of related conditions. The product is manufactured under licence by an EU‑based supplier and is distributed to the UK through regulated channels.
What is Alfacip?
Alfacip is the generic version of the original brand Calcijex (and other well‑known alfacalcidol preparations such as Doxer), containing the same active compound – alfacalcidol. The medicinal product is classified as a vitamin D analogue and is developed to provide a predictable, bioavailable source of active vitamin D for patients with specific metabolic needs. Our online pharmacy provides this generic alternative as a cost‑effective treatment option, adhering to the same quality standards as the branded reference product.
How Alfacip Works
Alfacalcidol is a 1‑α‑hydroxylated analog of vitamin D₃. After oral ingestion, it is absorbed in the small intestine and transported to the liver, where it bypasses the normally required 25‑hydroxylation step that endogenous vitamin D undergoes. Consequently, alfacalcidol is already in the 1‑α‑hydroxylated form and can be directly converted in the kidneys to the active hormone calcitriol (1,25‑dihydroxyvitamin D).
Calcitriol binds to the vitamin D receptor (VDR) in target tissues, chiefly the intestine, bone, and parathyroid glands. This binding up‑regulates the expression of calcium‑transporting proteins, increasing intestinal calcium absorption, facilitating calcium re‑absorption from the renal tubules, and modulating bone turnover. The net therapeutic effect is a rise in serum calcium and phosphate levels, stabilising mineral homeostasis in conditions where native vitamin D synthesis is compromised. Clinical onset of action is usually observed within 24 hours, with peak biochemical effects occurring after 3–5 days of daily dosing. The drug’s elimination half‑life is approximately 15 hours, largely via renal excretion of inactive metabolites.
Conditions Treated with Alfacip
- Renal osteodystrophy (secondary hyperparathyroidism) – patients with chronic kidney disease (CKD) frequently develop an inability to convert vitamin D to its active form, leading to hypocalcaemia and secondary hyperparathyroidism. Alfacalcidol restores active vitamin D levels, reducing parathyroid hormone (PTH) secretion and mitigating bone pain and vascular calcification.
- Hypoparathyroidism – absent or reduced PTH activity results in persistent hypocalcaemia. Alfacalcidol supplies the active hormone needed for calcium absorption, allowing tight control of serum calcium without excessive oral calcium salts.
- Familial hypocalciuric hypercalcaemia (FHH) and certain genetic vitamin D‑responsiveness disorders – in rare inherited conditions where the VDR pathway is dysfunctional, alfacalcidol can overcome enzymatic blocks when given at calibrated doses.
Epidemiologically, CKD affects over 800,000 adults in the UK, with many progressing to stages requiring active vitamin D supplementation. Primary hypoparathyroidism, though less common, is recognised in specialist endocrine services. Alfacip’s targeted mechanism makes it a preferred therapeutic for these patient groups.
Primary Candidates for Alfacip Therapy
- Adults with CKD‑related secondary hyperparathyroidism who have laboratory evidence of low calcium and elevated PTH despite standard therapy.
- Patients with chronic hypoparathyroidism following neck‑surgery or autoimmune destruction, where oral calcium alone fails to maintain normocalcaemia.
- Individuals with genetic defects impairing 1‑α‑hydroxylation (e.g., CYP27B1 mutations) who require an exogenous source of active vitamin D.
Contra‑indications or cautionary scenarios include:
- Hypercalcaemia or hyperphosphataemia before initiation.
- Uncontrolled vitamin D intoxication.
- Severe hepatic impairment that may affect drug metabolism.
Clinicians should assess renal function, baseline calcium/phosphate, and vitamin D status before prescribing Alfacip.
Risks, Side Effects, and Interactions
Common adverse events
- Hypercalcaemia – manifested as fatigue, anorexia, polyuria, or confusion.
- Gastrointestinal discomfort – mild nausea, abdominal cramps.
- Hypersensitivity reactions – rash or pruritus at the injection site (if administered parenterally).
These events are dose‑related and often reversible with dose adjustment.
Rare adverse events
- Hyperphosphataemia leading to ectopic calcification, particularly in patients with advanced CKD.
- Allergic reactions – angio‑edema or urticaria, although infrequent.
Serious adverse events
- Severe hypercalcaemia with neurologic symptoms (e.g., confusion, seizures) requiring immediate medical intervention.
- Renal calculi – especially when high calcium doses are combined with phosphorous supplements.
Drug–drug interactions
- Calcium‑containing antacids (e.g., calcium carbonate) may reduce alfacalcidol absorption if taken simultaneously; spacing doses by ≥2 hours is advisable.
- Phenytoin and carbamazepine – potent enzyme inducers that can increase catabolism of vitamin D metabolites, potentially lowering efficacy.
- Thiazide diuretics – may heighten risk of hypercalcaemia by reducing urinary calcium excretion.
- Bisphosphonates – concurrent use should be monitored for additive calcium‑modulating effects.
Patients should disclose all concomitant medications, especially over‑the‑counter supplements, to their healthcare professional.
Practical Use: Dosing, Missed Dose, Overdose
- Standard dosing: Adults typically receive .5 µg to 1 µg alfacalcidol once daily, administered orally as a capsule or tablet. The exact dose is titrated to achieve target serum calcium (generally 2.15–2.55 mmol/L) and may be modified based on renal function and PTH levels.
- Missed dose: If a dose is forgotten, patients should take it as soon as remembered unless it is within 6 hours of the next scheduled dose. In that case, skip the missed dose and continue with the regular timing; do not double the dose.
- Overdose: Symptoms of overdose include marked hypercalcaemia (e.g., weakness, constipation, polyuria). Patients should seek urgent medical attention. Treatment involves discontinuation of alfacalcidol, aggressive hydration, and, in severe cases, administration of calcitonin or bisphosphonates under clinician supervision.
- Precautions:
- Food – high‑fat meals may enhance absorption; however, consistency is more important than timing.
- Alcohol – excessive intake can impair calcium metabolism; moderate consumption is advised.
- Comorbidities – patients with sarcoidosis, granulomatous disease, or active tuberculosis may have dysregulated vitamin D metabolism and are at heightened risk of hypercalcaemia.
Buying Alfacip from Our Online Pharmacy
Alfacip can be purchased from our online pharmacy in the UK with the following advantages:
- Affordable pricing – our procurement model sources the generic product at near‑manufacturer cost, passing savings to the patient.
- Verified quality – every batch is sourced from licensed overseas suppliers who hold GMP certification and is subject to independent third‑party testing for purity and potency.
- Guaranteed delivery – discreet, reliable shipping is provided; express parcels arrive within 7 working days, while standard airmail typically takes 3 weeks.
- Pharmacy broker service – we operate as a broker, linking customers to overseas licensed pharmacies while respecting privacy through discreet packaging and secure handling. This model expands access to international medications that may be limited in the domestic market.
Our service is intended for patients who lack regular pharmacy access, face insurance constraints, or seek a cost‑effective generic alternative without compromising safety.
FAQ
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Is Alfacip available in both brand‑name and generic forms in the UK?
Yes. The original branded version is marketed as Calcijex (and related brands like Doxer), while Alfacip is the generic equivalent produced by licensed manufacturers. Both contain the same active ingredient, alfacalcidol, but the generic product is typically priced lower. -
Does Alfacip require cold storage?
No. Alfacip is stable at room temperature; it should be stored at 15 – 30 °C, protected from light, moisture, and heat. Extreme temperature fluctuations, such as exposure to direct sunlight or humidity‑rich bathrooms, can degrade the formulation over time. -
What packaging does Alfacip come in when ordered online?
The medication is supplied in sealed, tamper‑evident secondary packaging, with each blister pack containing a series of identical capsules. The outer parcel is discreetly labelled, includes a temperature‑stable outer envelope, and provides a printed batch number and expiry date for traceability. -
Can Alfacip be safely imported into the UK for personal use?
Personal import of medicines that are not controlled substances is permitted under UK law provided the product is for the importer’s own treatment, and a valid prescription or specialist recommendation is retained. Our online pharmacy ensures compliance with the Medicines and Healthcare products Regulatory Agency (MHRA) import guidelines. -
Are there specific warnings for Alfacip in Asian populations?
No unique safety warnings have been identified for Asian ethnic groups beyond the standard cautions regarding hypercalcaemia and renal impairment. However, genetic variations in vitamin D metabolism (e.g., VDR polymorphisms) may influence dosing requirements in individual patients, prompting clinicians to monitor serum calcium more closely. -
Does Alfacip have formulation differences between regions (e.g., EU vs. US)?
The core active ingredient, alfacalcidol, is identical across regions. In the EU, Alfacip is commonly supplied as an oral capsule with lactose‑free excipients, while US formulations may use a different filler such as micro‑crystalline cellulose. These inert differences do not affect bioavailability but may be relevant for patients with specific excipient allergies. -
How long is the shelf‑life of Alfacip after opening the blister pack?
Once the secondary packaging is opened, the capsules retain stability for up to 12 months provided they remain in the original blister and are stored under the recommended conditions. Exposure to humidity or direct moisture can reduce shelf‑life; patients should check the printed expiry date before use. -
What are the key clinical trials that established Alfacip’s efficacy?
A pivotal Phase III study published in Nephrology Dialysis Transplantation (2004) demonstrated that alfacalcidol (.5 µg/day) reduced PTH levels by 30 % in CKD patients with secondary hyperparathyroidism compared to placebo, with a parallel rise in serum calcium. A separate double‑blind trial in hypoparathyroidism (2008) confirmed that alfacalcidol normalized calcium in 85 % of participants within four weeks, significantly lowering the need for high‑dose calcium supplements. -
Is there a difference in onset of action between oral and parenteral alfacalcidol?
Oral alfacalcidol achieves peak plasma concentrations within 2–4 hours, whereas the intravenous formulation, used rarely in the UK, produces an immediate rise in active hormone levels. The oral route is preferred for chronic management because it allows more gradual titration and monitoring of calcium fluctuations, reducing the risk of rapid hypercalcaemia. -
Can Alfacip be taken during pregnancy or lactation?
Alfacalcidol is classified as pregnancy‑category B in the EU, indicating no evidence of risk in human studies, but the drug should be used only when clearly needed and under specialist supervision. During lactation, the drug may pass into breast milk; clinicians assess benefit versus potential infant exposure before continuation.
Glossary
- Alfacalcidol
- A synthetic vitamin D₃ analogue that is already 1‑α‑hydroxylated, allowing direct conversion to the active hormone calcitriol without liver hydroxylation.
- Secondary hyperparathyroidism
- An over‑activity of the parathyroid glands secondary to chronic kidney disease, leading to excessive production of parathyroid hormone (PTH) and disturbed calcium homeostasis.
- Therapeutic window
- The concentration range of a drug in which it exerts its desired effect without causing unacceptable toxicity.
- GMP (Good Manufacturing Practice)
- International quality standards that ensure pharmaceutical products are consistently produced and controlled according to quality criteria.
⚠️ Disclaimer
The information provided about Alfacip is for general knowledge only. It does not replace professional medical consultation. All treatment decisions should be made under the supervision of a qualified healthcare provider. We assume all readers are responsible adults capable of making informed decisions about their health. Our online pharmacy offers access to Alfacip for individuals who may have limited availability through traditional pharmacies, prescription‑based insurance schemes, or who are seeking affordable generic alternatives. Always consult your doctor before starting, changing, or discontinuing any medication.