No clinically important drug interactions have been identified. 'Proscar' does not appear to significantly affect the cytochrome P450-linked drug metabolising enzyme system. Compounds which have been tested in man include propranolol, digoxin, glibenclamide, warfarin, theophylline, and antipyrine and no clinically meaningful interactions were found.
Other concomitant therapy: Although specific interaction studies were not performed in clinical studies, 'Proscar' was used concomitantly with ACE inhibitors, alpha-blockers, beta-blockers, calcium-channel blockers, cardiac nitrates, diuretics, H2 antagonists, HMG-CoA reductase inhibitors, non-steroidal anti-inflammatory drugs (NSAIDs) including aspirin and paracetamol, quinolones and benzodiazepines without evidence of clinically significant adverse interactions
HBarca said:There are no clinically significant interactions between finasteride or to my knowledge dutasteride with alcohol, from the summary product characteristics data sheet (for finasteride):
[/quote
No, there defintiely are:
"There was also evidence that finasteride antagonized some alcohol effects, particularly among A-allele homozygotes... These findings are consistent with the results of studies in rodents, which show that the pregnane neuroactive steroids, especially ALLO, mediate some of the effects of acute alcohol administration"
http://www.nature.com/npp/journal/v30/n6/full/1300688a.html
antonio666 said:i seem to get pissed more easy...
Bryan said:antonio666 said:i seem to get pissed more easy...
Oh, dutasteride makes you ANGRY?
jakeb said:HBarca said:There are no clinically significant interactions between finasteride or to my knowledge dutasteride with alcohol, from the summary product characteristics data sheet (for finasteride):
[/quote
No, there defintiely are:
"There was also evidence that finasteride antagonized some alcohol effects, particularly among A-allele homozygotes... These findings are consistent with the results of studies in rodents, which show that the pregnane neuroactive steroids, especially ALLO, mediate some of the effects of acute alcohol administration"
http://www.nature.com/npp/journal/v30/n6/full/1300688a.html
I don't believe you are interpreting the results of this correctly,
In this study, we also examined the effects of finasteride, a 5AR inhibitor, on the subjective response to a moderate dose of alcohol in social drinkers. As hypothesized, finasteride reduced a number of the self-reported stimulant effects of alcohol, as measured by two subscales of the Alcohol SS (ie the Central-Stimulant and Dynamic-Peripheral Subscales), as well as the Stimulation Subscale of the BAES. These findings are consistent with the results of studies in rodents, which show that the pregnane neuroactive steroids, especially ALLO, mediate some of the effects of acute alcohol administration (Morrow et al, 1999, 2001). In rats, the time course of the alcohol-induced increase in brain ALLO concentration paralleled the appearance of specific behavioral and electrophysiological effects of alcohol (Finn et al, 2004; VanDoren et al, 2000), which were reversed by finasteride (VanDoren et al, 2000; Khisti et al, 2003).
Finasteride also reduced the numbing effects of alcohol, as measured by the SS Anesthetic Subscale. The mechanisms implicated in the numbing effects of alcohol are not as well understood as the general anesthetic effects. A recent study suggests that neuroactive steroids contribute to the hypnotic effects of ethanol in rats (Khisti et al, 2003). Moreover, several studies (Mihic et al, 1997; Koltchine et al, 1999; Mascia et al, 2000; Ueno et al, 2001) have suggested that general anesthesia can be produced, at least in part, by enhancing neuronal inhibition mediated by the GABAA alpha-2 subunit.