In Stock

Mono®Femara (Letrozole)

$90.00

ACTIVE INGREDIENT: LETROZOLE 2.5
TABLET COUNT: 50 COUNTS
ACTIVE HALF-LIFE: 9 HOURS
CLASSIFICATION: ANTI ESTROGEN
DOSAGE MEN: 2.5/DAY
DOSAGE WOMEN: 2.5/DAY
ACNE: NONE
WATER RETENTION: NO
HBR: NO
HEPATOXITY: LOW
AROMATIZATION: NO

Compare
SKU: MF1 Category: Tags: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

Description

Buy Mono®Femara (Letrozole) Online.

Mono®Femara (Letrozole) is the medication for certain types of breast cancer in women after menopause. Buy steroids online if you want to prevent cancer from returning. king pen flavors

Letrozole, as its main ingredient decreases the amount of estrogen the body makes. This is to prevent some breast cancers from growing faster.

Dosage Forms And Strengths

2.5 mg tablets: dark yellow, film-coated, round, slightly biconvex, with beveled edges (imprinted with the letters FV on one side and CG on the other side).

Storage And Handling

Packaged in HDPE bottles with a safety screw cap.

2.5 mg tablets

Bottles of 30 tablets – NDC 0078-0249-15

Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].

Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reactions rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

Adjuvant Treatment Of Early Breast Cancer

In study, BIG 1-98, the median treatment duration of adjuvant treatment was 60 months and the median duration of follow-up for safety was 96 months for patients receiving Femara and tamoxifen.

Certain adverse reactions were prospectively specified for analysis (see Table 1), based on the known pharmacologic properties and side effect profiles of the two drugs.

Adverse reactions were analyzed irrespective of whether a symptom was present or absent at baseline. Most adverse reactions reported (approximately 75% of patients who reported AEs) were Grade 1 or Grade 2 applying the Common Toxicity Criteria (CTC) Version 2.0/Common Terminology Criteria for Adverse Events (CTCAE), Version 3.0. Table 1 describes adverse reactions (Grades 1-4 and Grades 3-4) irrespective of relationship to study treatment in the adjuvant trial for the monotherapy arms analysis (safety population).

Reviews

There are no reviews yet.

Be the first to review “Mono®Femara (Letrozole)”

Your email address will not be published. Required fields are marked *