Sildenafilo Salutas Uses

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What is Sildenafilo Salutas?

Sildenafilo Salutas is used to treat men who have erectile dysfunction (also called sexual impotence). Sildenafilo Salutas belongs to a group of medicines called phosphodiesterase 5 (PDE5) inhibitors. These medicines prevent an enzyme called phosphodiesterase type-5 from working too quickly. The penis is one of the areas where this enzyme works.

Erectile dysfunction is a condition where the penis does not harden and expand when a man is sexually excited, or when he cannot keep an erection. When a man is sexually stimulated, his body's normal response is to increase blood flow to his penis to produce an erection. By controlling the enzyme, Sildenafilo Salutas helps to maintain an erection after the penis is stroked. Without physical action to the penis, such as that occurring during sexual intercourse, Sildenafilo Salutas will not work to cause an erection.

Sildenafilo Salutas is also used in both men and women to treat the symptoms of pulmonary arterial hypertension. This is a type of high blood pressure that occurs between the heart and the lungs. When hypertension occurs in the lungs, the heart must work harder to pump enough blood through the lungs. Sildenafilo Salutas works on the PDE5 enzyme in the lungs to relax the blood vessels. This will increase the supply of blood to the lungs and reduce the workload of the heart.

Sildenafilo Salutas is available only with your doctor's prescription.

Sildenafilo Salutas indications

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Sildenafilo Salutas is indicated for the treatment of pulmonary arterial hypertension (WHO Group I) in adults to improve exercise ability and delay clinical worsening. The delay in clinical worsening was demonstrated when Sildenafilo Salutas was added to background epoprostenol therapy.

Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with New York Heart Association (NYHA) Functional Class II–III symptoms and idiopathic etiology (71%) or associated with connective tissue disease (CTD) (25%).

Limitation of Use: Adding Sildenafilo Salutas to bosentan therapy does not result in any beneficial effect on exercise capacity.

How should I use Sildenafilo Salutas?

Use Sildenafilo Salutas suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Sildenafilo Salutas suspension.

Uses of Sildenafilo Salutas in details

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Use: Labeled Indications

Erectile dysfunction: Sildenafilo Salutas: Treatment of erectile dysfunction.

Pulmonary arterial hypertension: Sildenafilo Salutas: Treatment of pulmonary arterial hypertension (WHO group I; efficacy established predominately in patients with WHO/NYHA functional class II and III) in adults to improve exercise ability and delay clinical worsening.

Off Label Uses

High-altitude pulmonary edema

Based on the 2019 Wilderness Medical Society consensus guidelines for the prevention and treatment of acute altitude illness, Sildenafilo Salutas is a recommended option for the prevention and treatment of high-altitude pulmonary edema (as an adjunct to descent, oxygen, or portable hyperbaric therapy). Supplemental oxygen and descent are the mainstays of treatment. For prevention, Sildenafilo Salutas should only be considered for patients with a history of high-altitude pulmonary edema, especially multiple episodes.

Raynaud phenomenon

Data from a meta-analysis and small controlled trials support the use of Sildenafilo Salutas for Raynaud phenomenon related to systemic sclerosis, demonstrating a decrease in the frequency and severity of attacks.

Sildenafilo Salutas description

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Each film-coated tablet contains Sildenafil citrate equivalent to 50 mg Sildenafilo Salutas.

Each film-coated tablet contains Sildenafil citrate equivalent to 100 mg Sildenafilo Salutas.

Each orodispersible tablet contains Sildenafil citrate equivalent to 50 mg Sildenafilo Salutas.

Excipients/Inactive Ingredients: Film-Coated Tablets: In addition to the active ingredient, Sildenafilo Salutas citrate, each tablet contains the following inactive ingredients: Microcrystalline cellulose, calcium hydrogen phosphate (anhydrous), croscarmellose sodium, magnesium stearate, hydroxypropyl methylcellulose (hypromellose), titanium dioxide (E171), lactose, triacetin, and FD & C Blue #2 aluminum lake [indigo carmine aluminum lake (E132)].

Orodispersible Tablets: In addition to the active ingredient, Sildenafilo Salutas citrate, each orodispersible tablet contains the following inactive ingredients: Microcrystalline cellulose, silica hydrophobic colloidal, croscarmellose sodium, magnesium stearate, indigo carmine aluminium lake (E132), sucralose, mannitol, crospovidone, polyvinyl acetate, povidone, flavouring (contains: Maltodextrin and dextrin), natural flavouring (contains: Maltodextrin, E422 glycerol and E1520 propylene glycol), lemon flavouring (contains: Maltodextrin and E307 alpha tocopherol).

Sildenafilo Salutas dosage

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Sildenafilo Salutas Dosage

Generic name: Sildenafilo Salutas CITRATE 20mg

Dosage form: tablet, film coated; injection; oral powder

The information at Drugs.com is not a substitute for medical advice. Always consult your doctor or pharmacist.

Sildenafilo Salutas Tablets and

Oral Suspension

The recommended dose of Sildenafilo Salutas is 5 mg or 20 mg three times a day. Administer Sildenafilo Salutas doses 4–6 hours apart.

In the clinical trial no greater efficacy was achieved with the use of higher doses. Treatment with doses higher than 20 mg three times a day is not recommended.

Sildenafilo Salutas Injection

Sildenafilo Salutas injection is for the continued treatment of patients with PAH who are currently prescribed oral Sildenafilo Salutas and who are temporarily unable to take oral medication.

The recommended dose is 2.5 mg or 10 mg administered as an intravenous bolus injection three times a day. The dose of Sildenafilo Salutas injection does not need to be adjusted for body weight.

A 10 mg dose of Sildenafilo Salutas injection is predicted to provide pharmacological effect of Sildenafilo Salutas and its N-desmethyl metabolite equivalent to that of a 20 mg oral dose.

Reconstitution of the Powder for

Oral Suspension

  1. Tap the bottle to release the powder.
  2. Remove the cap.
  3. Accurately measure out 60 mL of water and pour the water into the bottle. (Figure 1)

    Figure 1

  4. Replace the cap and shake the bottle vigorously for a minimum of 30 seconds. (Figure 2)

    Figure 2

  5. Remove the cap.
  6. Accurately measure out another 30 mL of water and add this to the bottle. You should always add a total of 90 mL of water irrespective of the dose prescribed. (Figure 3)

    Figure 3

  7. Replace the cap and shake the bottle vigorously for a minimum of 30 seconds. (Figure 4)

    Figure 4

  8. Remove the cap.
  9. Press the bottle adaptor into the neck of the bottle (as shown on Figure 5, below). The adaptor is provided so that you can fill the oral syringe with medicine from the bottle. Replace the cap on the bottle.

    Figure 5

  10. Write the expiration date of the constituted oral suspension on the bottle label (the expiration date of the constituted oral suspension is 60 days from the date of constitution).

Incompatibilities

Do not mix with any other medication or additional flavoring agent.

More about Sildenafilo Salutas (Sildenafilo Salutas)

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Sildenafilo Salutas interactions

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What other drugs will affect Sildenafilo Salutas?

Effects of Other Drugs on Sildenafilo Salutas Sildenafilo Salutas Citrate

In Vitro Studies: Sildenafilo Salutas Sildenafilo Salutas metabolism is principally mediated by the cytochrome P450 (CYP) isoforms 3A4 (major route) and 2C9 (minor route). Therefore, inhibitors of these isoenzymes may reduce Sildenafilo Salutas clearance.

In Vivo Studies: Cimetidine (800 mg), a nonspecific CYP inhibitor, caused a 56% increase in plasma Sildenafilo Salutas concentrations when coadministered with Sildenafilo Salutas citrate (50 mg) to healthy volunteers.

When a single 100 mg dose of Sildenafilo Salutas citrate was administered with erythromycin, a specific CYP3A4 inhibitor, at steady state (500 mg bid for 5 days), there was a 182% increase in Sildenafilo Salutas systemic exposure (AUC). In addition, coadministration of the HIV protease inhibitor saquinavir, also a CYP3A4 inhibitor, at steady state (1200 mg tid) with Sildenafilo Salutas citrate (100 mg single dose) resulted in a 140% increase in Sildenafilo Salutas Cmax and a 210% increase in Sildenafilo Salutas AUC. Sildenafilo Salutas Sildenafilo Salutas citrate had no effect on saquinavir pharmacokinetics. Stronger CYP3A4 inhibitors such as ketoconazole or itraconazole would be expected to have still greater effects, and population data from patients in clinical trials did indicate a reduction in Sildenafilo Salutas clearance when it was coadministered with CYP3A4 inhibitors (such as ketoconazole, erythromycin, or cimetidine).

Coadministration with the HIV protease inhibitor ritonavir, which is a highly potent P450 inhibitor, at steady state (400 mg bid) with Sildenafilo Salutas citrate (100 mg single dose) resulted in a 300% (4-fold) increase in Sildenafilo Salutas Cmax and a 1000% (11-fold) increase in Sildenafilo Salutas plasma AUC. At 24 hours the plasma levels of Sildenafilo Salutas were still approximately 200 ng/mL, compared to approximately 5 ng/mL when Sildenafilo Salutas was dosed alone. This is consistent with ritonavirs marked effects on a broad range of P450 substrates. Sildenafilo Salutas Sildenafilo Salutas citrate had no effect on ritonavir pharmacokinetics.

It can be expected that concomitant administration of CYP3A4 inducers, such as rifampin, will decrease plasma levels of Sildenafilo Salutas.

Single doses of antacid (magnesium hydroxide/aluminum hydroxide) did not affect the bioavailability of Sildenafilo Salutas citrate.

Pharmacokinetic data from patients in clinical trials showed no effect on Sildenafilo Salutas pharmacokinetics of CYP2C9 inhibitors (such as tolbutamide, warfarin), CYP2D6 inhibitors (such as selective serotonin reuptake inhibitors, tricyclic antidepressants), thiazide and related diuretics, ACE inhibitors, and calcium channel blockers. The AUC of the active metabolite, N-desmethyl Sildenafilo Salutas, was increased 62% by loop and potassium-sparing diuretics and 102% by nonspecific beta-blockers. These effects on the metabolite are not expected to be of clinical consequence.

Effects of Sildenafilo Salutas Sildenafilo Salutas Citrate on Other Drugs

In Vitro Studies: Sildenafilo Salutas Sildenafilo Salutas is a weak inhibitor of the cytochrome P450 isoforms 1A2, 2C9, 2C19, 2D6, 2E1 and 3A4 (IC50 >150 mM). Given Sildenafilo Salutas peak plasma concentrations of approximately 1 mcM after recommended doses, it is unlikely that Sildenafilo Salutas citrate will alter the clearance of substrates of these isoenzymes.

In Vivo Studies: When Sildenafilo Salutas citrate 100 mg oral was coadministered with amlodipine, 5 mg or 10 mg oral, to hypertensive patients, the mean additional reduction on supine blood pressure was 8 mmHg systolic and 7 mmHg diastolic.

No significant interactions were shown with tolbutamide (250 mg) or warfarin (40 mg), both of which are metabolized by CYP2C9.

Sildenafilo Salutas Sildenafilo Salutas citrate (50 mg) did not potentiate the increase in bleeding time caused by aspirin (150 mg).

Sildenafilo Salutas Sildenafilo Salutas citrate (50 mg) did not potentiate the hypotensive effect of alcohol in healthy volunteers with mean maximum blood alcohol levels of 0.08%.

Sildenafilo Salutas Sildenafilo Salutas (100 mg) did not affect the steady state pharmacokinetics of the HIV protease inhibitors, saquinavir and ritonavir, both of which are CYP3A4 substrates.

Sildenafilo Salutas side effects

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What are the possible side effects of Sildenafilo Salutas?

The following serious adverse events are discussed elsewhere in the labeling:

Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction 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.

Safety data of Sildenafilo Salutas in adults were obtained from the 12-week, placebo-controlled clinical study (Study 1) and an open-label extension study in 277 Sildenafilo Salutas-treated patients with PAH, WHO Group I.

The overall frequency of discontinuation in Sildenafilo Salutas-treated patients on 20 mg three times a day was 3% and was the same for the placebo group.

In Study 1, the adverse reactions that were reported by at least 3% of Sildenafilo Salutas-treated patients (20 mg three times a day) and were more frequent in Sildenafilo Salutas-treated patients than in placebo-treated patients are shown in Table 1. Adverse reactions were generally transient and mild to moderate in nature.

Table 1: Most Common Adverse Reactions in Patients with PAH in Study 1 (More Frequent in Sildenafilo Salutas-Treated Patients than Placebo-Treated Patients and Incidence ≥ 3% in Sildenafilo Salutas-Treated Patients)

Placebo, %

(n = 70)

Sildenafilo Salutas 20 mg three times a day, %

(n = 69)

Placebo-Subtracted, %
Epistaxis 1 9 8
Headache 39 46 7
Dyspepsia 7 13 6
Flushing 4 10 6
Insomnia 1 7 6
Erythema 1 6 5
Dyspnea exacerbated 3 7 4
Rhinitis 0 4 4
Diarrhea 6 9 3
Myalgia 4 7 3
Pyrexia 3 6 3
Gastritis 0 3 3
Sinusitis 0 3 3
Paresthesia 0 3 3

At doses higher than the recommended 20 mg three times a day, there was a greater incidence of some adverse reactions including flushing, diarrhea, myalgia and visual disturbances. Visual disturbances were identified as mild and transient, and were predominately color-tinge to vision, but also increased sensitivity to light or blurred vision.

The incidence of retinal hemorrhage with Sildenafilo Salutas 20 mg three times a day was 1.4% versus 0% placebo and for all Sildenafilo Salutas doses studied was 1.9% versus 0% placebo. The incidence of eye hemorrhage at both 20 mg three times a day and at all doses studied was 1.4% for Sildenafilo Salutas versus 1.4% for placebo. The patients experiencing these reactions had risk factors for hemorrhage including concurrent anticoagulant therapy.

In a placebo-controlled fixed dose titration study (Study 2) of Sildenafilo Salutas (starting with recommended dose of 20 mg and increased to 40 mg and then 80 mg all three times a day) as an adjunct to intravenous epoprostenol in patients with PAH, the adverse reactions that were more frequent in the Sildenafilo Salutas + epoprostenol group than in the epoprostenol group (greater than 6% difference) are shown in Table 2.

Table 2: Adverse Reactions (%) in patients with PAH in Study 2 (incidence in Sildenafilo Salutas + Epoprostenol group at least 6% greater than Epoprostenol group)

Sildenafilo Salutas + Epoprostenol

(n = 134)

Epoprostenol

(n = 131)

(Sildenafilo Salutas + Epoprostenol) minus Epoprostenol
Headache 57 34 23
Edema^ 25 13 14
Dyspepsia 16 2 14
Pain in extremity 17 6 11
Diarrhea 25 18 7
Nausea 25 18 7
Nasal congestion 9 2 7
^includes peripheral edema

Sildenafilo Salutas Injection

Sildenafilo Salutas injection was studied in a 66-patient, placebo-controlled study in patients with PAH at doses targeting plasma concentrations between 10 and 500 ng/mL (up to 8 times the exposure of the recommended dose). Adverse events with Sildenafilo Salutas injection were similar to those seen with oral tablets.

Postmarketing Experience

The following adverse reactions have been identified during post approval use of Sildenafilo Salutas (marketed for both PAH and erectile dysfunction). Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Cardiovascular Events

In postmarketing experience with Sildenafilo Salutas at doses indicated for erectile dysfunction, serious cardiovascular, cerebrovascular, and vascular events, including myocardial infarction, sudden cardiac death, ventricular arrhythmia, cerebrovascular hemorrhage, transient ischemic attack, hypertension, pulmonary hemorrhage, and subarachnoid and intracerebral hemorrhages have been reported in temporal association with the use of the drug. Most, but not all, of these patients had preexisting cardiovascular risk factors. Many of these events were reported to occur during or shortly after sexual activity, and a few were reported to occur shortly after the use of Sildenafilo Salutas without sexual activity. Others were reported to have occurred hours to days after use concurrent with sexual activity. It is not possible to determine whether these events are related directly to Sildenafilo Salutas, to sexual activity, to the patient's underlying cardiovascular disease, or to a combination of these or other factors.

Nervous system

Seizure, seizure recurrence

Sildenafilo Salutas contraindications

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What is the most important information I should know about Sildenafilo Salutas?

Do not take Sildenafilo Salutas if you are also using a nitrate drug for chest pain or heart problems. This includes nitroglycerin (Nitrostat, Nitrolingual, Nitro-Dur, Nitro-Bid, and others), isosorbide dinitrate (Dilatrate-SR, Isordil, Sorbitrate), and isosorbide mononitrate (Imdur, ISMO, Monoket). Nitrates are also found in some recreational drugs such as amyl nitrate or nitrite ("poppers"). Taking Sildenafilo Salutas with a nitrate medicine can cause a sudden and serious decrease in blood pressure.

During sexual activity, if you become dizzy or nauseated, or have pain, numbness, or tingling in your chest, arms, neck, or jaw, stop and call your doctor right away. You could be having a serious side effect of Sildenafilo Salutas.

Do not take Sildenafilo Salutas more than once a day. Allow 24 hours to pass between doses. Do not take Sildenafilo Salutas while also taking Sildenafilo Salutas, unless your doctor tells you to.

Contact your doctor or seek emergency medical attention if your erection is painful or lasts longer than 4 hours. A prolonged erection (priapism) can damage the penis.

Sildenafilo Salutas can decrease blood flow to the optic nerve of the eye, causing sudden vision loss. This has occurred in a small number of people taking Sildenafilo Salutas, most of whom also had heart disease, diabetes, high blood pressure, high cholesterol, or certain pre-existing eye problems, and in those who smoke or are over 50 years old. It is not clear whether Sildenafilo Salutas is the actual cause of vision loss.

Stop using Sildenafilo Salutas and get emergency medical help if you have sudden vision loss.



Active ingredient matches for Sildenafilo Salutas:

Sildenafil in Netherlands.


List of Sildenafilo Salutas substitutes (brand and generic names)

Sort by popularity
Unit description / dosage (Manufacturer)Price, USD
Sildora film-coated tab 100 mg 4's (Synmedic)
Sildora film-coated tab 50 mg 4's (Synmedic)$ 5.73
SILNAFIL 25 MG TABLET 1 strip / 10 tablets each (Emcure Pharmaceuticals Ltd)$ 2.17
Silnafil 25mg Tablet (Emcure Pharmaceuticals Ltd)$ 0.24

References

  1. PubChem. "sildenafil". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  2. DrugBank. "sildenafil". http://www.drugbank.ca/drugs/DB00203 (accessed September 17, 2018).
  3. MeSH. "Urological Agents". https://www.ncbi.nlm.nih.gov/mesh/68... (accessed September 17, 2018).

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