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Rozgra Dosage |
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Generic name: Rozgra 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.
The recommended dose of Rozgra is 5 mg or 20 mg three times a day. Administer Rozgra 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.
Rozgra injection is for the continued treatment of patients with PAH who are currently prescribed oral Rozgra 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 Rozgra injection does not need to be adjusted for body weight.
A 10 mg dose of Rozgra injection is predicted to provide pharmacological effect of Rozgra and its N-desmethyl metabolite equivalent to that of a 20 mg oral dose.
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Incompatibilities
Do not mix with any other medication or additional flavoring agent.
Do not use Rozgra with Viagra similar medications such as avanafil (Stendra), tadalafil (Cialis) or vardenafil (Levitra). Tell your doctor about all medications you use for erectile dysfunction.
Many drugs can interact with Rozgra. Not all possible interactions are listed here. Tell your doctor about all your medications and any you start or stop using during treatment with Rozgra, especially:
an antibiotic such as clarithromycin, erythromycin, rifampin, or telithromycin;
antifungal medication such as itraconazole, ketoconazole, miconazole, posaconazole, or voriconazole;
drugs to treat high blood pressure or a prostate disorder, such as alfuzosin, doxazosin, prazosin, terazosin, silodosin, tamsulosin;
heart or blood pressure medication such as amlodipine, diltiazem, nicardipine, quinidine, or verapamil;
the hepatitis C medications boceprevir or telaprevir; or
HIV/AIDS medicine such as atazanavir, darunavir, fosamprenavir, indinavir, nelfinavir, ritonavir, saquinavir, or tipranavir.
This list is not complete and many other drugs can interact with Rozgra. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Give a list of all your medicines to any healthcare provider who treats you.
Effects of Other Drugs on Rozgra Viagra Citrate
In Vitro Studies: Rozgra Viagra metabolism is principally mediated by the cytochrome P450 (CYP) isoforms 3A4 (major route) and 2C9 (minor route). Therefore, inhibitors of these isoenzymes may reduce Rozgra clearance.
In Vivo Studies: Cimetidine (800 mg), a nonspecific CYP inhibitor, caused a 56% increase in plasma Rozgra concentrations when coadministered with Rozgra (50 mg) to healthy volunteers.
When a single 100 mg dose of Rozgra was administered with erythromycin, a specific CYP3A4 inhibitor, at steady state (500 mg bid for 5 days), there was a 182% increase in Rozgra systemic exposure (AUC). In addition, coadministration of the HIV protease inhibitor saquinavir, also a CYP3A4 inhibitor, at steady state (1200 mg tid) with Rozgra (100 mg single dose) resulted in a 140% increase in Rozgra Cmax and a 210% increase in Rozgra AUC. Rozgra Viagra 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 Rozgra 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 Rozgra (100 mg single dose) resulted in a 300% (4-fold) increase in Rozgra Cmax and a 1000% (11-fold) increase in Rozgra plasma AUC. At 24 hours the plasma levels of Rozgra were still approximately 200 ng/mL, compared to approximately 5 ng/mL when Rozgra was dosed alone. This is consistent with ritonavirs marked effects on a broad range of P450 substrates. Rozgra Viagra 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 Rozgra.
Single doses of antacid (magnesium hydroxide/aluminum hydroxide) did not affect the bioavailability of Rozgra.
Pharmacokinetic data from patients in clinical trials showed no effect on Rozgra 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 Rozgra, 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 Rozgra Viagra Citrate on Other Drugs
In Vitro Studies: Rozgra Viagra is a weak inhibitor of the cytochrome P450 isoforms 1A2, 2C9, 2C19, 2D6, 2E1 and 3A4 (IC50 >150 mM). Given Rozgra peak plasma concentrations of approximately 1 mcM after recommended doses, it is unlikely that Rozgra will alter the clearance of substrates of these isoenzymes.
In Vivo Studies: When Rozgra 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.
Rozgra Viagra citrate (50 mg) did not potentiate the increase in bleeding time caused by aspirin (150 mg).
Rozgra Viagra citrate (50 mg) did not potentiate the hypotensive effect of alcohol in healthy volunteers with mean maximum blood alcohol levels of 0.08%.
Rozgra Viagra (100 mg) did not affect the steady state pharmacokinetics of the HIV protease inhibitors, saquinavir and ritonavir, both of which are CYP3A4 substrates.
Users | % | ||
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Once in a day | 1 | 100.0% |
Users | % | ||
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51-100mg | 1 | 33.3% | |
11-50mg | 1 | 33.3% | |
101-200mg | 1 | 33.3% |
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Information checked by Dr. Sachin Kumar, MD Pharmacology
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