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CialisAka: Tadalafil
- Indications
- Contraindications
- Absolute Contraindications (risk of hypotension)
- Men using nitrates (i.e. Nitroglycerin)
- Men using alpha blockers (e.g. Hytrin for BPH)
- Relative Contraindications
- Active coronary ischemia in men not on nitrates
- Congestive Heart Failure
- Borderline low Blood Pressure
- Bordrline low volume status
- Multidrug antihypertensive regimen
- Taking Cytochrome P450-3A4 (CYP3A4) inhibitor
- Absolute Contraindications (risk of hypotension)
- Mechanism
- Pharmacokinetics
- Onset within 30 to 60 minutes
- Duration as long as 36 hours
- Contrast with 4 hours with Viagra
- Prolonged effect also leads to prolonged side effects
- Dosing
- Start 20 mg PO 1 hour before intercourse
- Do not take more than once per 2 days
- Most insurance limits to 6 per month
- Indications to start with half dosing (10 mg)
- Age over 65 years
- Hepatic Impairment
- Renal Impairment
- Concurrent use of Cytochrome P3A4 inhibitor below
- Start 20 mg PO 1 hour before intercourse
- Drug Interactions
- Inhibit breakdown of Viagra via Cytochrome P3A4
- Cimetidine (Tagamet)
- Erythromycin
- Ketoconazole (Nizoral)
- Itraconazole (Sporonox)
- Mibefradil (Posicor)
- Profound Vasodilitation and Hypotension (Avoid)
- Nitrates
- Alpha-blockers (use Tamsulosin instead)
- Inhibit breakdown of Viagra via Cytochrome P3A4
- Adverse Effects
- References
Cialis (C0967376) | |
|---|---|
| Concepts | Organic Chemical (T109) , Pharmacologic Substance (T121) |
| MSH | C429886 |
| English | Cialis, Lilly brand of tadalafil |
| Parent Concepts | Moved elsewhere (C1274021) |
| Sources | MSH, MTH, NCI, PDQ, RXNORM, SCTSPA, SNOMEDCT Derived from the NIH UMLS (Unified Medical Language System) |
tadalafil (C1176316) | |
|---|---|
| Definition (NCI) | A carboline-based compound with vasodilatory properties. Tadalafil selectively inhibits the cyclic guanosine monophosphate (cGMP)-specific type 5 phosphodiesterase- (PDE-5)-mediated degradation of cGMP, which is found in the smooth muscle of the corpus cavernosa and corpus spongiosum of the penis. Inhibition of cGMP degradation by tadalafil results in prolonged muscle relaxation, vasodilation, and blood engorgement of the corpus cavernosa, thereby prolonged penile erection. |
| Definition (PDQ) | A carboline-based compound with vasodilatory properties. Tadalfil selectively inhibits the cyclic guanosine monophosphate (cGMP)-specific type 5 phosphodiesterase- (PDE-5)-mediated degradation of cGMP, which is found in the smooth muscle of the corpus cavernosa and corpus spongiosum of the penis. Inhibition of cGMP degradation by tadalfil results in prolonged muscle relaxation, vasodilation, and blood engorgement of the corpus cavernosa, and, so, prolonged penile erection. Check for "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=462366&idtype=1" active clinical trials or "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=462366&idtype=1&closed=1" closed clinical trials using this agent. ("http://nciterms.nci.nih.gov:80/NCIBrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C47743" NCI Thesaurus) |
| Concepts | Organic Chemical (T109) , Pharmacologic Substance (T121) |
| MSH | C429886 |
| English | tadalafil, TADALAFIL @ @ UNIDENTIFIED, TADALAFIL UNIDENTIFIED |
| Spanish | tadalafil |
| Parent Concepts | Phosphodiesterase Inhibitors (C0031638), Antispasmodics (C0037766), Smooth muscle relaxant (C0304437), Phosphodiesterase 5 inhibitor (C1318700), Genital system agent (C1320003) |
| Sources | MSH, MTHSPL, NCI, PDQ, RXNORM, SCTSPA, SNOMEDCT, USPMG, VANDF Derived from the NIH UMLS (Unified Medical Language System) |
