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  2. Trimethoprim/sulfamethoxazole - Wikipedia

    en.wikipedia.org/wiki/Trimethoprim/sulfamethoxazole

    Trimethoprim serves as a competitive inhibitor of dihydrofolate reductase (DHFR), hence inhibiting the de novo synthesis of tetrahydrofolate, the biologically active form of folate. [ 14 ] Tetrahydrofolate is crucial in the synthesis of purines , thymidine , and methionine which are needed for the production of DNA and proteins [ 28 ] during ...

  3. Isoniazid/pyridoxine/sulfamethoxazole/trimethoprim - Wikipedia

    en.wikipedia.org/wiki/Isoniazid/pyridoxine/sulfa...

    Other studies, however, have found fixed-dose combinations to be useful for this purpose. [2] References This page was last edited on 26 September ...

  4. ACE inhibitor - Wikipedia

    en.wikipedia.org/wiki/ACE_inhibitor

    A combination of ACE inhibitor with other drugs may increase effects of these drugs, but also the risk of adverse effects. [19] The commonly reported adverse effects of drug combination with ACE inhibitor are acute renal failure, hypotension, and hyperkalemia. The drugs interacting with ACE inhibitor should be prescribed with caution.

  5. Antibiotic synergy - Wikipedia

    en.wikipedia.org/wiki/Antibiotic_synergy

    A classic example of this effect is the interaction between β-lactams, which damage the bacteria cell membrane, and aminoglycosides, which inhibit protein synthesis. [1] The damage dealt to the cell wall by β-lactams allows more aminoglycoside molecules to be taken up into the cell than would otherwise be possible, enhancing cell damage. [ 1 ]

  6. Discovery and development of ACE inhibitors - Wikipedia

    en.wikipedia.org/wiki/Discovery_and_development...

    These results also indicate that the N-domain possess a broader selectivity than the C-domain. Another difference between the older ACE inhibitors and RXP 407 is the molecular size of the compound. The older ACE inhibitors had mostly been interacting with S 1 ’, S 2 ’ and S 1 subsites but RXP 407 interacts in addition with the S 2 subsite.

  7. Sulfamethoxazole - Wikipedia

    en.wikipedia.org/wiki/Sulfamethoxazole

    Its Tmax (or time to reach maximum drug concentration in plasma) occurs 1 to 4 hours after oral administration. The mean serum half-life of sulfamethoxazole is 10 hours. [8] However, the half-life of the drug noticeably increases in people with creatinine clearance rates equal to or less than 30 mL/minute.

  8. Drug interaction - Wikipedia

    en.wikipedia.org/wiki/Drug_interaction

    When two drugs affect each other, it is a drugdrug interaction (DDI). The risk of a DDI increases with the number of drugs used. [1] A large share of elderly people regularly use five or more medications or supplements, with a significant risk of side-effects from drugdrug interactions. [2] Drug interactions can be of three kinds ...

  9. Moexipril - Wikipedia

    en.wikipedia.org/wiki/Moexipril

    Moexipril was an angiotensin converting enzyme inhibitor (ACE inhibitor) [1] used for the treatment of hypertension and congestive heart failure. Moexipril can be administered alone or with other antihypertensives or diuretics. [2] It works by inhibiting the conversion of angiotensin I to angiotensin II. [3]

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