Product Details:
| Minimum Order Quantity | 10 Strip |
| Dose/Strength | 2.5 mg |
| Usage/Application | Personal |
| Brand | Letroz |
| Packaging Size | 5x5 |
| Packaging Type | Box |
| Country of Origin | Made in India |
Additional Information:
Product Details:
| Minimum Order Quantity | 10 Strip |
| Dose/Strength | 2.5 mg |
| Usage/Application | Personal |
| Brand | Letronol 2.5 Tablet |
| Packaging Size | 10x10 |
| Packaging Type | Box |
| Medicine Type | Allopathic |
| Country of Origin | Made in India |
Letrozole 2.5 mg tablet is a prescription oral medication classified as a non-steroidal aromatase inhibitor. It is primarily used in women with hormone-sensitive breast cancer and off-label in fertility treatments and bodybuilding for estrogen control.
Letrozole blocks the aromatase enzyme, which converts androgens (testosterone) into estrogens in fat and other tissues.
By inhibiting estrogen synthesis, it helps slow or prevent the growth of estrogen receptor–positive (ER+) tumors.
Each tablet contains 2.5 mg of letrozole.
Usually comes in strip packs of 5 or 10 tablets.
Common Indian brands: Femara, Letoval, Letroz, Letronat, Letz.
| Condition | Effect |
|---|---|
| Hormone-sensitive breast cancer in postmenopausal women | Prevents recurrence, slows growth |
| Adjuvant therapy | Used after surgery/radiation to prevent relapse |
| Neoadjuvant therapy | To shrink tumors before surgery |
| Use | Why It’s Used |
|---|---|
| Ovulation induction (in women with PCOS or infertility) | Stimulates ovulation by reducing estrogen feedback |
| Bodybuilding | Controls estrogen from anabolic steroid use (prevents gynecomastia and water retention) |
| Male infertility | Increases FSH/LH by lowering estrogen, thus boosting testosterone |
Inhibits aromatase → ↓ estrogen synthesis
In women, less estrogen slows growth of ER+ breast cancer
In men, lower estrogen → increased LH/FSH → ↑ testosterone
In fertility, reduced estrogen feedback → pituitary releases more FSH → stimulates ovulation
2.5 mg once daily (long-term therapy, often 5 years)
2.5 to 7.5 mg/day from day 3 to 7 of the menstrual cycle
Sometimes higher doses (up to 12.5 mg) under specialist supervision
0.25 to 2.5 mg, 2–3 times/week
Dose depends on steroid cycle strength and estrogen conversion potential
Used with testosterone-based steroid cycles to prevent:
Gynecomastia
Bloating / water retention
Mood swings / estrogen rebound
| Drug | Class | Potency | Use in Bodybuilding |
|---|---|---|---|
| Letrozole | Non-steroidal AI | Very strong | Strong estrogen control, crash risk |
| Anastrozole | Non-steroidal AI | Moderate | Common in TRT and mild cycles |
| Exemestane | Steroidal AI | Moderate–High | Has some androgenic activity |
Hot flashes
Vaginal dryness
Bone thinning (osteoporosis)
Fatigue
Joint pain
Mood swings
Additional Information:
Product Details:
| Minimum Order Quantity | 10 Strip |
| Strength | 1 mg |
| Packaging Size | 30 Tablets |
| Packaging Type | 1x30 tablet |
| Brand | SiroBoon 1 mg |
| Manufacturer | Kachhela |
| Country of Origin | Made in India |
Sirolimus Tablets (Rapamycin)
Sirolimus is an immunosuppressant drug, mainly used to prevent organ transplant rejection and sometimes in certain rare diseases or cancers.
🔹 CompositionActive ingredient: Sirolimus (various strengths, usually 1 mg, 2 mg, or higher depending on brand).
Dosage form: Oral tablets.
Sirolimus is an mTOR (mammalian target of rapamycin) inhibitor.
It works by blocking T-cell and B-cell activation and proliferation (immune cells responsible for attacking transplanted organs).
Unlike calcineurin inhibitors (like Tacrolimus or Cyclosporine), it does not cause nephrotoxicity directly but can affect kidney function indirectly.
Primary use:
Prevention of kidney transplant rejection (often used with corticosteroids and cyclosporine initially, then sometimes as maintenance therapy).
Other uses (off-label/rare):
Certain rare cancers and tumors (e.g., renal cell carcinoma, Kaposi’s sarcoma).
Lymphangioleiomyomatosis (LAM): a rare lung disease, especially in women.
Research use in anti-aging/longevity medicine (not officially approved).
Kidney transplant:
Loading dose: ~6 mg orally, followed by maintenance dose of 2 mg daily.
Adjusted according to blood trough levels (therapeutic drug monitoring is essential).
Dose always individualized by the transplant physician.
Taken consistently with or without food (but always the same way each time for steady absorption).
Common:
Mouth ulcers / sores.
High cholesterol and triglycerides.
Anemia, low platelet counts.
Delayed wound healing.
Swelling in legs (peripheral edema).
Diarrhea, abdominal pain.
Serious (require monitoring):
Infections (due to suppressed immunity).
Interstitial lung disease (rare but serious).
Kidney function impairment (especially if combined with cyclosporine).
Hepatic artery thrombosis (in liver transplant – contraindicated).
Increased risk of certain cancers (lymphoma, skin cancer).
Sirolimus blood levels (trough concentration monitoring).
Kidney function tests (serum creatinine).
Liver function tests.
Lipid profile (cholesterol, triglycerides).
Blood counts.
Hypersensitivity to sirolimus.
Use in liver and lung transplants (associated with higher complication risk).
Pregnancy and breastfeeding (safety not established).
Metabolized by CYP3A4 enzyme and P-glycoprotein.
Many drug interactions (e.g., ketoconazole, clarithromycin, rifampicin, anticonvulsants, grapefruit juice) → can greatly change sirolimus blood levels.
Avoid live vaccines during therapy.
Protect from sun (higher skin cancer risk).
Regular monitoring is mandatory.
Additional Information: