procainamide वाक्य
उदाहरण वाक्य
मोबाइल
- All patients had previously not responded to an antiarrhythmic drug called procainamide.
- Also it binds 10 % less to proteins than procainamide.
- Procainamide, quinidine and disopyramide are Class Ia agents.
- Also procainamide-induced antinuclear antibodies are formed after a 6 months treatment.
- Chemically, it is the " N "-acetylated metabolite of procainamide.
- This substitution is the reason why procainamide exhibit a longer half-life time than procaine.
- It is a Class III antiarrhythmic agent, whereas procainamide is a Class Ia antiarrhythmic drug.
- Oral procainamide is no longer being manufactured in the US, but intravenous formulations are still available.
- Procainamide is structurally similar to procaine but in place of an ester group contains procainamide an amide group.
- Procainamide is structurally similar to procaine but in place of an ester group contains procainamide an amide group.
- Other drugs used for ventricular arrhythmia include lidocaine, amiodarone, bretylium, flecainide, procainamide, and mexiletine.
- People with atrial fibrillation and rapid ventricular response are often treated with amiodarone or procainamide to stabilize their heart rate.
- Also procainamide can be acetylated to acecainide and to other reactive and toxic metabolites, which would contradict the efficacy.
- "' Procainamide "'is a medication of the antiarrhythmic class used for the treatment of cardiac arrhythmias.
- To have a high efficacy, the antiarrhythmic drug procainamide has to be dosed frequently to maintain an adequate serum concentration.
- It is only partially as active as procainamide; when checking levels, both must be included in the final calculation.
- But further research showed, that after a long-term therapy of procainamide, some subjects did not produce any antinuclear antibodies.
- Brodie also did research on anesthetic and hypnotic drugs and discovered that procainamide was effective in treating patients with severe irregularities in heart rhythm.
- Both propoxyphene and norpropoxyphene are potent blockers of cardiac membrane sodium channels and are more potent than lidocaine, quinidine, and procainamide in this respect.
- Procainamide is a classical bioisostere because the valence electron structure of a disubstituted oxygen atom is the same as a trisubstituted nitrogen atom, as Langmuir showed.
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