Buy Cyclessa from Canadian & International Pharmacies
Cyclessa (Desogestrel/Ethinyl Estradiol)and/or alternatives
General Information on Cyclessa
Cyclessa is a combination of two generic drugs- ethinyl estradiol and desogestrel. This combination is used as a contraceptive to prevent a pregnancy.
Ethinyl estradiol and desogestrel are a mix of female hormones that stop the process of ovulation. By preventing the process of ovulation, Cyclessa is able to avoid a pregnancy.
Cyclessa also causes certain changes to occur in the uterine lining and cervical mucus. These changes make it harder for the sperm to penetrate the uterus and for the fertilized egg to attach itself to the uterine wall.
Side effects of Cyclessa
Cyclessa is not to be taken if you are already pregnant or recently gave birth. The risk of adverse side effects increases if you suffer from circulation problems caused especially by diabetes, hormonal cancer, breast cancer, uterine cancer, liver cancer, any other liver disease, abnormal vaginal bleeding, severe hypertension, heart valve disorders, or migraine headaches. You must also not take Cyclessa if you have a history of blood clots, strokes, or jaundice due to birth control pills.
The use of Cyclessa or any other hormonal drug increases the risk of strokes, blood clots, and heart attacks in patients who smoke or are equal to or older than 35 years of age. Serious side effects could occur on taking Cyclessa. These side effects include the appearance of breast lumps, dark urine, swelling of the feet, ankles, and hands, low fever, nausea, stomach pain, loss of appetite, clay colored stools, jaundice, heaviness or pain in the chest that spreads to the arms and shoulders, and changes in the severity or pattern of migraine headaches.
Mild side effects could include vaginal itching or unusual discharge, changes in appetite and weight, freckles, breast pain, darkening of facial skin, swelling, tenderness, mild nausea, bloating, vomiting, stomach cramps, changes in menstrual cycle, reduced sex drive, dizziness, nervousness, tiredness, and headaches.
Dosage of Cyclessa
Cyclessa is available in the form of oral tablets in a 28-day blister back. The treatment cycle of 28 days is divided into 4 dosing phases. 7 rounded and yellow tablets are for the first phase, 7 rounded and orange tablets are for the second phase, 7 rounded and red tablets are for the third phase, and 7 rounded and green tablets are for the last phase. The green colored tablets for the last phase contain no active ingredients.
This dosing period is recommended to begin during the first day of the period or the first Sunday after the period begins. During the first few days of using Cyclessa, additional birth control measures such as a spermicide or condom may have to be used.
Breakthrough bleeding may be seen during the first 3 months after you start taking Cyclessa. However, you must inform your doctor if the bleeding becomes severe.
Buy Cyclessa from North Drug Store
You can buy Cyclessa from North Drug Store, an online prescription service that offers several generic and branded drugs at very affordable rates. All prescription drug orders are handled by qualified pharmacists, making it a safe place to buy drugs online.
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What is a "Generic" medication/drug?
Generic drugs are medications that have the comparable medicinal ingredients as the original brand name drug, but which are generally cheaper in price. Nearly 1 in 3 drugs dispensed are "generic". They undergo comparative testing to ensure that they are the same as their "brand" counterparts in:
- Active Ingredient (e.g. "Pravastatin" is the active ingredient in brand name Pravachol)
- Dosage (e.g. 10 mg of the active ingredient)
- Safety (e.g. same or similar side effects, drug interactions)
- Performance (e.g. 10 mg of a "generic" can be substituted for 10 mg of the "brand" and have the same therapeutic result)
- Intended use (e.g. both "generic" and "brand" would be prescribed for the same conditions)
What this means is that "generic" medications can be used as a substitute of their brand equivalents with comparable therapeutic results. There are a few exceptions (examples are outlined at the end of this page) and as always you should consult your physician before switching from a brand name medications to a generic or vice versa.
What differences are there between generic and brand?
While generics and brand equivalent drugs contain comparable active ingredients, they may be different in the following ways:
- Appearance (e.g. the scoring or markings)
The color, shape and size of the medication come from the fillers that are added to the active ingredients to make the drug. These fillers that are added to the drug have no medical use and do not to change the effectiveness of the final product. A generic drug must contain comparable active ingredients and must be comparable in strength and dosage to the original brand name equivalent. Generic drugs can be more cost effective than purchasing the brand name.
Why do generics cost less than the brand name equivalents?
When a new drug is "invented", the company that discovered it has a patent on it that gives them the exclusive production rights for this medication. Once the patent expires in a country, other companies can bring the product to market under their own name. This patent prevents other companies from copying the drug during that time so they can earn back their Research and Development costs through being the exclusive supplier of the product. After the patent expires however, other companies can develop a "generic" version of the product. These versions generally are offered at much lower prices because the companies do not have the same development costs as the original company who developed the medication.
The main thing to realize here though is that the two products are therapeutically comparable. They may look different, and be called something different, but they are required to be have the same active ingredient.
How are Generic drugs tested to ensure quality and efficacy?
The two most generally accepted methods to prove the safety of a generic version of a drug are to either repeat most of the chemistry, animal and human studies originally done, or to show that the drug performs comparably with the original brand name drug. This second option is called a "comparative bioavailability" study. During this type of study, volunteers are given the original drug, and then separately later the generic drug. The rates at which the drug is delivered to the patient (into their blood stream or otherwise absorbed) are measured to ensure they are the same. Because the same active ingredient is used the major concern is just that it delivers the common chemical(s) at the same rate so that they have the same effect. Please note that the methods that the manufacturers use may vary from country to country.