Yarina Plus

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Yarina Plus

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Yarina Plus

Property Description
Active Ingredients Drospirenone, Ethinylestradiol, Calcium Levomefolinate
Form Oral Film-coated Tablet
Pharmacological Class Combined Oral Contraceptive (COC) and Folate Supplement
Common Use Prevention of Pregnancy (Contraception)
Origin Synthetic (Hormones) and Semi-Synthetic (Folate)

Yarina Plus is a Combined Oral Contraceptive (COC) preparation, which means it is a medication that utilizes two types of synthetic hormones for pregnancy prevention, delivered in an oral film-coated tablet dosage form. As a combination product, it belongs to the pharmacological class of ovulation controlling agents, and its primary therapeutic use is effective contraception for females of reproductive potential. Combined hormonal contraceptives are a recognized method for fertility regulation. This mechanism of action is characterized by providing control over the reproductive cycle, a key benefit for individuals seeking predictable prevention of pregnancy.


Composition: Drospirenone, Ethinylestradiol, and Folate

The core composition of Yarina Plus involves three distinct active ingredients: the synthetic progestogen Drospirenone (DRSP), the synthetic estrogenic compound Ethinylestradiol (EE), and the B-vitamin component Calcium Levomefolinate. The Drospirenone and Ethinylestradiol work in tandem to achieve the primary purpose of contraception by controlling the reproductive cycle.

A unique feature that differentiates this formula is the inclusion of Calcium Levomefolinate, which is an active, readily bioavailable form of folate. This third component is included for the general benefit of improvement in folate status, supplementing the essential B-vitamin within the body, which is involved in cell processes. This is a differentiating factor compared to traditional COCs, providing complementary nutritional support alongside pregnancy prevention.

What side effects are possible with Yarina Plus?

Possible Side Effects and Safety Information

The safety profile for this combined oral contraceptive (COC) is formally structured across several domains, as defined by regulatory authorities.


Documented Adverse Reactions and Frequency

Adverse reactions are classified based on incidence observed in clinical trials. Reactions reported as most frequent (Very Common or Common, ge2% incidence) often include symptoms affecting multiple System-Organ Classes (SOCs), such as Headache/Migraine, nausea or vomiting, breast pain or tenderness, mood changes, and menstrual irregularities.

Time-related safety patterns officially documented include the expectation of unscheduled bleeding or spotting, which is more frequently reported during the first three months of use.


Serious Safety Considerations

The most significant safety concern documented in regulatory labeling is the risk of thromboembolic events, particularly Venous Thromboembolism (VTE), which includes Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE). The risk of VTE is officially documented as highest during the first year of use or upon restarting a COC after a break of four weeks or more.

Other serious adverse reactions include Arterial Thrombotic Events (e.g., Stroke, Myocardial Infarction), the development of Hepatic Tumors, and the potential for Hyperkalemia (elevated serum potassium), which is linked to the drospirenone component.


Population-Specific Constraints

The product is contraindicated (should not be used) in women with a history of renal impairment or adrenal insufficiency due to the risk of Hyperkalemia. Safety warnings also exist for women over 35 years of age who smoke, as this combination significantly increases the risk of serious cardiovascular events, requiring strict regulatory caution.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory documentation for Yarina Plus, which contains Drospirenone and Ethinylestradiol, specifies the documented clinical manifestations that may occur following the ingestion of multiple tablets in excess of the prescribed dose. The acute, observable signs typically reported within the gastrointestinal system include nausea and vomiting. A common effect on the reproductive system following acute overdose in adult females is the occurrence of withdrawal vaginal bleeding, reflecting the effect of the hormones.

The established protocol mandates immediate medical attention for any suspected overdose scenario. Individuals are formally instructed to contact a local Poison Help line or seek medical help right away upon recognizing these symptoms or confirming excessive ingestion, as this is a required emergency action defined in the prescribing information. This urgent response is necessary to ensure proper assessment.

Management of an overdose event is officially classified as symptomatic and supportive. This therapeutic approach is followed because regulatory sources state that no specific antidote is known to counteract the effects of the hormonal components of this combined oral contraceptive. Furthermore, the regulatory label notes a population-specific consideration: slight vaginal bleeding is a potential manifestation that may occur in young girls following the accidental ingestion of the hormonal tablets.

Therapeutic Uses of Yarina Plus

What Yarina Plus Treats: Main Uses and Benefits

Yarina Plus is commonly used across three primary therapeutic domains, contributing to symptom management and pregnancy prevention. It is applied in addressing distressing symptoms and conditions characterized by periods of heightened manifestations.

The therapeutic relevance of this medication spans conditions presenting with disruptive symptom manifestations, notably Premenstrual Dysphoric Disorder (PMDD), specific skin conditions, and the core indication of pregnancy prevention. In clinical settings marked by increased discomfort or tension, Yarina Plus helps address pronounced symptomatic manifestations. This includes managing severe mood swings, irritability, depressed mood, and cyclic bloating associated with PMDD, and may assist with managing symptom intensity of disruptive menstrual symptoms like heavy flow or pain.

“This treatment is relevant when supportive symptom management is appropriate, especially for conditions involving episodic or fluctuating manifestations.”

The combined hormonal component is considered relevant for skin conditions marked by heightened symptoms of moderate acne, and is used for managing the manifestations of inflammatory and non-inflammatory lesions. The inclusion of a readily available folate component provides a distinct supportive benefit, and may assist with supporting general well-being during symptomatic phases of long-term hormonal therapy.


Quick Fact: Relief for Cyclic Distress

Yarina Plus is commonly used to help with the severe emotional and physical symptoms of PMDD, providing support that helps patients cope more steadily during difficult, recurring premenstrual episodes.

Regulatory References

  1. National Library of Medicine's DailyMed overview

Eligibility and Restrictions for Use

Official Eligibility Rules for Yarina Plus

The eligibility for using Yarina Plus is strictly defined by regulatory authorities and centers on avoiding serious health risks, primarily thrombotic events and complications related to the drug's hormonal and mineralocorticoid activity. The medicine is primarily intended for females of reproductive potential.


Absolute Contraindications (Must Not Use)

Population/Condition Regulatory Basis
High Risk of Thrombosis History of DVT, PE, stroke, or severe hypercoagulopathies.
Age and Smoking Females over 35 years of age who smoke cigarettes.
Organ Dysfunction Liver disease, liver tumors, renal impairment, or adrenal insufficiency.
Hormone-Sensitive Cancer Current or history of breast cancer or other estrogen/progestin-sensitive cancer.
Pregnancy Known or suspected pregnancy.

Restricted and Conditional Use

Use is not recommended for nursing mothers (lactation) due to potential effects on milk production. Furthermore, the medicine is not indicated for the geriatric population. Eligibility for the acne indication begins in women at least 14 years of age who have achieved menarche. Use is restricted following major surgery, requiring discontinuation at least four weeks prior to the procedure.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The interaction profile of Yarina Plus is defined by pharmacokinetic and pharmacodynamic mechanisms as documented in regulatory labeling. Official documentation establishes clear restrictions and prohibitions for co-administration with specific substances.

Contraindicated Combinations and Conditions

Co-administration with certain Hepatitis C regimens, specifically combinations containing Ombitasvir, Paritaprevir, and Ritonavir, is strictly prohibited due to the risk of significant elevation in liver enzymes. Fezolinetant is also contraindicated, as the Ethinylestradiol component substantially increases its systemic exposure. Use is formally contraindicated for women over 35 years of age who smoke, due to an increased risk of serious cardiovascular events.

Pharmacokinetic and Exposure Effects

Medicines classified as strong enzyme inducers, including certain anticonvulsants and the herbal product St. John’s wort, may decrease the plasma concentrations of Drospirenone and Ethinylestradiol. This effect is regulatory-cited as potentially reducing contraceptive effectiveness. Strong CYP3A4 inhibitors, such as Ketoconazole, may increase Drospirenone exposure, a pharmacokinetic effect requiring caution.

Pharmacodynamic and Folate Interactions

Due to Drospirenone’s anti-mineralocorticoid activity, co-administration with other potassium-raising agents—including potassium-sparing diuretics, ACE inhibitors, and chronic use of NSAIDs—creates a documented risk of hyperkalemia. This risk leads to contraindications for patients with renal impairment or adrenal insufficiency when co-administering these agents. Certain drugs, such as Methotrexate, may also interfere with the metabolism and availability of the Calcium Levomefolinate component.

Mechanism of Action

The mechanism of Yarina Plus is executed through three distinct pharmacological actions: central hormonal feedback, peripheral receptor antagonism, and metabolic supplementation.

Central Hormonal Feedback Ethinyl Estradiol ( estrogen agonist) and Drospirenone ( progestin agonist) exert negative feedback on hypothalamic and pituitary receptors. This suppresses GnRH secretion, preventing the LH and FSH surges necessary for follicular development. The result is anovulation (prevention of egg release), alongside physical changes that thicken cervical mucus and alter the endometrium.

Peripheral Receptor Antagonism Drospirenone acts as an antagonist at the Mineralocorticoid Receptors ( MR) in the kidney and at Androgen Receptors ( AR) in peripheral tissues. MR antagonism opposes the action of aldosterone, leading to a mild natriuretic and diuretic effect. AR antagonism reduces sebum production, decreasing androgen-mediated activity in the skin.

Metabolic Support The inclusion of Levomefolate Calcium provides the biologically active folate ( 5-methyltetrahydrofolate), which enters the one-carbon metabolism pathway. This mechanism ensures the maintenance of adequate folate concentrations essential for DNA synthesis and cellular function.

Dosage and Administration Information

How to Use Yarina Plus: Administration Guidelines

Yarina Plus (Drospirenone, Ethinylestradiol, and Levomefolate Calcium) is administered according to a strict, continuous 28-day cyclic regimen. The medication is delivered exclusively via the oral route, taken as one tablet daily.


Administration Scope and Regimen

The standard dosing involves taking one tablet daily for 28 consecutive days, using a course that typically includes 24 active/folate combination tablets followed by 4 hormone-free folate tablets. This regimen establishes a fixed sequence that must be maintained throughout the cycle. The tablet should be taken at the same time every day to ensure consistency in the daily schedule. Intake may occur with or without food.


Procedural Instructions

Instruction Domain Requirement
Starting the Cycle Initiation may be carried out using either the Day 1 Start (first day of menses) or the Sunday Start method.
Tablet Order Tablets must be taken in the exact, sequential order directed on the blister pack to ensure the correct transition between the hormonal and non-hormonal components.
Missed Dose Specific procedural guidance is provided for managing missed active tablets, which may require the use of supplemental, non-hormonal contraception for a designated period to maintain the cycle’s integrity.
Age-Specific Use The product is indicated for use in females who have achieved menarche, including for the management of moderate acne in women at least 14 years of age.

Connection to the Overall Use Protocol

This procedural structure establishes a mandatory 28-day cyclic administration pattern using oral, once-daily, fixed-time dosing. The instructions emphasize sequential intake and strict adherence to the time of day, creating a regimen that is repeated continuously. The included age-specific guidance and missed-dose protocols define the procedural boundaries for both initiating and maintaining the administration schedule.

Recent Clinical Evidence

Research evidence / Overview of Studies for Yarina Plus

Research exploring how this medication is studied for pregnancy prevention has utilized large-scale study designs, including intermediate-term, non-comparative randomized clinical trials and large post-marketing observational studies focused on healthy women of reproductive potential. These studies monitor the rate of pregnancy incidence and cycle control patterns. Regulatory reports described the measured outcomes as aligning with the established parameters for a hormonal contraceptive product. The core evidence focuses on how the method performs under controlled study conditions; however, long-term data for rare events rely primarily on non-randomized observational studies.

The medication was studied for its application in managing symptoms associated with Premenstrual Dysphoric Disorder (PMDD) using short-term, randomized, placebo-controlled trials. These trials measured changes in patient-reported outcomes for affective and physical symptoms. The duration of the observed patterns for PMDD has not been evaluated when the medication is used for more than three menstrual cycles, providing limited information for long-term outcomes or sustained symptom management.

The hormonal combination was evaluated in trials for its potential role in managing symptoms of moderate acne vulgaris, tracking outcomes such as inflammatory and non-inflammatory lesion counts over typically six menstrual cycles. Research predominantly focused on moderate facial acne, with limited published study information focused specifically on severe forms of acne.

The inclusion of the folate component was confirmed via pharmacokinetic/pharmacodynamic (PK/PD) trials, which observed an increase in folate biomarker concentrations over the intermediate term. However, no dedicated clinical trial has been conducted to directly evaluate the effect of the product on reducing the actual incidence of neural tube defects (NTDs). The final public health outcome related to the incidence of NTDs is an inference drawn from the established scientific evidence linking folate status to reduced risk.

Frequently Asked Questions (FAQ)

Common questions about Yarina Plus (FAQ)

Q: What is the main difference between Yarina Plus and a standard birth control pill?

A: Yarina Plus contains two hormones—drospirenone and ethinyl estradiol—which are common to many oral contraceptives. Its key difference is that it contains levomefolate calcium, a form of folic acid, in addition to the two hormones. This component is not typically present in standard combined pills.

Q: Does Yarina Plus contain the same active ingredients as Yaz or Yasmin?

A: Yarina Plus contains the same two hormonal ingredients, drospirenone and ethinyl estradiol, that are found in both Yaz and Yasmin. Official information describes the key difference as the inclusion of the third active ingredient, levomefolate calcium (a form of folic acid), in Yarina Plus.

Q: Is Yarina Plus used for anything other than preventing pregnancy?

A: According to official product information, Yarina Plus is also indicated for two other specific medical uses in women who choose an oral contraceptive. These uses are the treatment of moderate acne vulgaris and the treatment of symptoms associated with Premenstrual Dysphoric Disorder (PMDD).

Q: What are the benefits of the 'Plus' component in Yarina Plus?

A: The 'Plus' component is levomefolate calcium, a form of folic acid. Official documents describe the purpose of the levomefolate calcium as supporting folate status in women using oral contraception. It is noted as being a form of dietary supplement within the medication.

Q: Do the inactive pills in Yarina Plus contain any vitamins or active substances?

A: Yes, the pills taken during the hormone-free interval (inactive pills) contain levomefolate calcium (a form of folic acid). This component is an active substance, but the pills do not contain any hormones.

Q: Does Yarina Plus make you gain weight?

A: Official labeling, based on clinical trials, reports that increased weight has been noted as a potential adverse reaction. This is one of many possible effects described in the regulatory documents.

Q: Can Yarina Plus affect your mood or cause anxiety?

A: Official reports on adverse reactions state that mood changes and affect lability (unstable or rapidly changing mood) have been reported in clinical trials for this type of medication.

Q: Is spotting or breakthrough bleeding common when first starting Yarina Plus?

A: Official warnings and precautions mention that unscheduled bleeding or spotting sometimes occurs. This is commonly reported during the initial adjustment period, specifically the first three months of starting the medication.

Q: Are headaches a frequent side effect reported with Yarina Plus?

A: Yes, according to adverse reaction data from clinical studies, both headache and migraine are among the most frequently reported adverse reactions associated with the use of this medication.

Q: What are the serious, but rare, side effects associated with Yarina Plus?

A: Serious risks described in official documents include the potential for venous thromboembolism (VTE) risk, arterial thrombotic events, certain liver tumors (hepatic adenomas), and the risk of developing hyperkalemia (high potassium levels) in women with certain pre-existing conditions.

Q: Does taking Yarina Plus increase the risk of blood clots?

A: Official safety information confirms that all combined oral contraceptives are associated with an increased risk of venous thromboembolism (VTE). Regulatory warnings note that the VTE risk may differ between combined oral contraceptives based on the progestin type.

Q: Can antibiotics like amoxicillin reduce the effectiveness of Yarina Plus?

A: Official labeling advises caution with certain drugs classified as enzyme inducers, as they can decrease the pill's effectiveness. Common antibiotics like amoxicillin are generally not listed as enzyme inducers, the class of drugs that regulatory information emphasizes as interacting with the pill.

Q: Are there any herbal supplements that interact with Yarina Plus?

A: Official drug interaction information warns that certain supplements and medications that are CYP3A4 enzyme inducers may potentially lower the effectiveness of the pill. St. John's Wort is a known herbal example of an enzyme inducer mentioned in regulatory documents.

Q: Can using Yarina Plus affect liver function test results?

A: Yes, official warnings and precautions note that combined oral contraceptives have the potential to influence the results of certain laboratory tests. This includes tests related to liver function and other biochemical markers.

Q: Is Yarina Plus recommended for women who are close to menopause?

A: The medication is indicated for use in females of reproductive potential and is not indicated for use in elderly women. Official prescribing information notes that risk factors, particularly cardiovascular risk, are relevant considerations based on age.

Q: What are the reasons someone might have to stop taking Yarina Plus?

A: Official documents list several conditions that require evaluation and potential discontinuation. These include the occurrence of a thrombotic event (blood clot), the onset of a migraine with aura, uncontrolled high blood pressure, or diagnosis of a condition listed in the contraindications.

Q: Is there evidence about the long-term safety of using Yarina Plus?

A: Clinical trial data supports the safety profile for the approved indications. Long-term use of combined oral contraceptives is associated with a slight, rare increased risk for certain conditions, with the understanding that the overall benefit-risk profile is assessed by regulatory bodies for the intended use.

Q: What is the role of the drospirenone component in the medication?

A: Drospirenone is a progestin that acts by inhibiting ovulation. Official information also notes its anti-mineralocorticoid activity, which can affect water and potassium balance, and its anti-androgenic activity, which is linked to the treatment of acne.

Q: Does Yarina Plus help with menstrual pain or cramps?

A: While not an approved primary indication for pain relief, combined oral contraceptives are known to regulate and affect the menstrual cycle. This can influence menstrual symptoms.

Q: How does Yarina Plus affect acne?

A: Yarina Plus is specifically indicated in its official labeling for the treatment of moderate acne vulgaris in women who have chosen an oral contraceptive for birth control.

Q: Is it possible to take Yarina Plus continuously without a break?

A: The standard official product labeling describes a continuous 28-day cyclic regimen, which includes four hormone-free pills. This establishes the standard approved use pattern for this specific product.

Q: What is the difference in how Yarina Plus works compared to an IUD?

A: Yarina Plus is a systemic oral contraceptive that works primarily by stopping ovulation (release of an egg) and altering cervical mucus. An IUD is a local contraceptive device that works primarily within the uterus.

Q: Are there specific symptoms that require immediate medical attention while on Yarina Plus?

A: Yes, the official patient information provides clear warnings about signs of serious conditions. These include signs of blood clots (e.g., sudden severe chest or leg pain, vision changes) or hyperkalemia (e.g., muscle weakness) that require immediate medical evaluation.

Q: Do studies suggest Yarina Plus can affect fertility after stopping its use?

A: The medication's primary function is to suppress the monthly release of an egg (ovulation). Official documents generally do not suggest a permanent effect on the ability to become pregnant after a woman stops taking the medication.

Q: What is the general chemical classification of the hormones in Yarina Plus?

A: Yarina Plus is classified as a combined hormonal contraceptive. It contains a synthetic estrogen (ethinyl estradiol) and a progestin (drospirenone).

Q: What is the duration of the withdrawal bleed (period) typically experienced with Yarina Plus?

A: Official patient counseling suggests that withdrawal bleeding, which is similar to a menstrual period, usually begins within two to three days after the last hormone-containing active tablet is taken.

Q: Can Yarina Plus cause changes in appetite?

A: Changes in appetite are noted as features of Premenstrual Dysphoric Disorder (PMDD), for which the medication is indicated. This suggests a potential relationship with appetite regulation.

Q: Does Yarina Plus interact with thyroid medications?

A: Official warnings note that combined oral contraceptives can affect certain blood proteins called binding globulins. This may influence the dosage of thyroid hormone replacement therapy, which is why monitoring is typically required.

Q: What is the general guidance for taking Yarina Plus if I experience vomiting or severe diarrhea?

A: Official procedural guidance exists for managing active tablets in the event of severe vomiting or diarrhea occurring shortly after intake. This is due to the potential for reduced absorption of the active ingredients.

Q: Is Yarina Plus approved for use in women with a history of migraines?

A: Official documents state that this medication is contraindicated in women with a history of migraine with aura. For women with other types of migraines, any significant change or worsening of headaches requires prompt medical evaluation.

Q: Are there any known issues with taking Yarina Plus and certain cholesterol medications?

A: Official labeling advises that an alternate contraceptive method should be considered for women with uncontrolled dyslipidemias (abnormal lipid levels). This is because combined oral contraceptives may adversely affect cholesterol and triglyceride levels.

Q: What kind of research has been conducted on the effectiveness of Yarina Plus?

A: Official documents include a Clinical Studies section that summarizes the design and results of studies used to establish the drug’s effectiveness. These studies support its approved uses for contraception, acne, and PMDD.

Q: Does taking Yarina Plus affect blood pressure?

A: Yes, an increase in blood pressure has been reported in women taking combined oral contraceptives. The medication is contraindicated (should not be used) in women with uncontrolled high blood pressure.

Q: Is it true that the risk of blood clots is higher in the first year of using this type of pill?

A: Official safety documents indicate that the risk of developing venous thromboembolism (blood clots) is generally highest during the first year of use after a woman first starts or restarts a combined oral contraceptive.

Q: What is the typical timeframe for side effects like nausea to resolve after starting Yarina Plus?

A: Patient counseling information often suggests that common side effects, such as nausea and vomiting, may gradually subside or resolve within the first three months of use as the body adjusts to the medication.

Q: Does Yarina Plus offer any protection against sexually transmitted infections (STIs)?

A: No. The official patient information explicitly states that Yarina Plus, like all hormonal contraceptives, does not protect against HIV infection (AIDS) or any other sexually transmitted infections.

Q: What happens if I forget to take the inactive (vitamin) pills?

A: Official instructions state that missing the inactive, folate-only pills does not carry a risk of pregnancy. The guidance is to simply discard the missed pill(s) and continue taking one tablet daily to finish the pack.

Q: Are there any regulatory black box warnings associated with Yarina Plus?

A: Yes, combined hormonal contraceptives carry an FDA Black Box Warning. This serious warning concerns the increased risk of cardiovascular events in women who smoke cigarettes, especially those over 35 years of age.

Q: Do studies exist comparing different methods of contraception, including Yarina Plus?

A: Official information establishes the effectiveness of the drug itself. Patient information may sometimes refer to the fact that other methods of contraception, such as sterilization, are generally described as being more effective than oral contraceptives.

Q: What are the contraindications listed for using Yarina Plus?

A: The official product labeling lists several contraindications (reasons not to use the drug). These include a high risk of blood clots, certain hormone-sensitive cancers, liver disease or tumors, uncontrolled high blood pressure, and renal or adrenal insufficiency.

Q: Can certain anti-seizure medications affect the effectiveness of Yarina Plus?

A: Yes, the official labeling warns that medications that are CYP3A4 enzyme inducers, which include several anti-seizure drugs, may reduce the contraceptive effectiveness of the pill.

Q: How is the hormone level in Yarina Plus considered compared to older pills?

A: The ethinyl estradiol dose in Yarina Plus is described in official contexts as a low-dose estrogen formulation when compared to older generations of oral contraceptive pills that contained higher estrogen doses.

Q: Does Yarina Plus contain lactose or gluten?

A: Official labeling and patient information sheets indicate the presence of lactose as an excipient (non-active ingredient) in the tablets.

Q: Does Yarina Plus increase the risk of certain cancers?

A: The use of combined hormonal contraceptives is associated with a slight increase in the risk of certain conditions, including cervical cancer and a very rare risk of hepatic (liver) carcinoma.

How should Yarina Plus be stored and disposed of?

How to Store and Dispose of Yarina Plus?

The storage and disposal requirements for Yarina Plus are defined by regulatory labeling to maintain the stability of the active components (drospirenone, ethinyl estradiol, and levomefolate calcium).

Storage Conditions

Condition Requirement (Official Labeled Storage)
Temperature Store at 25 C (77 F), with permitted excursions between 15 C and 30 C (USP Controlled Room Temperature).
Protection Keep the blister strips in the original carton to protect the tablets from moisture and light until use.
Prohibited The product must not be frozen and must be kept out of the sight and reach of children.

Disposal Instructions

Unused or expired Yarina Plus should not be flushed down the toilet or poured down a drain. Disposal must be completed through an authorized drug take-back program or by following specific government guidelines for safe household trash disposal.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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