How do you administer this medicine?
Actions of Erisine in details
The action of the drug on the human body is called Pharmacodynamics in Medical terminology. To produce its effect and to change the pathological process that is happening the body and to reduce the symptom or cure the disease, the medicine has to function in a specific way. The changes it does to the body at cellular level gives the desired result of treating a disease. Drugs act by stimulating or inhibiting a receptor or an enzyme or a protein most of the times. Medications are produced in such a way that the ingredients target the specific site and bring about chemical changes in the body that can stop or reverse the chemical reaction which is causing the disease.
Orally administered Erisine stearate is readily and reliably absorbed. Optimal serum levels of Erisine are reached when the drug is taken in the fasting state or immediately before meals.
Erisine diffuses readily into most body fluids. Only low concentrations are normally achieved in the spinal fluid, but passage of the drug across the blood-brain barrier increases in meningitis. In the presence of normal hepatic function, Erisine is concentrated in the liver and excreted in the bile; the effect of hepatic dysfunction on excretion of Erisine by the liver into the bile is not known. Less than 5% of the orally administered dose of Erisine is excreted in active form in the urine.
Microbiology: Biochemical tests demonstrate Erisine inhibits protein synthesis of the pathogen without directly affecting nucleic acid synthesis. Antagonism has been demonstrated between clindamycin and Erisine.
Erisine binds to the 50S ribosomal subunits of susceptible bacteria and suppresses protein synthesis.
Erisine is usually active against most strains of the following organisms both in vitro and in clinical infections: Gram-Positive Organisms: Corynebacterium diphtheriae, Corynebacterium minutissimum, Listeria monocytogenes, Staphylococcus aureus (resistant organisms may emerge during treatment), Streptococcus pneumoniae, Streptococcus pyogenes.
Gram-Negative Organisms: Bordetella pertussis, Legionella pneumophilia, Neisseria gonorrhoeae.
Other Microorganisms: Chlamydia trachomatis, Entamoeba histolytica, Mycoplasma pneumoniae, Ureaplasma urealyticum.
Erisine has been shown to be active in vitro against most strains of the following organisms; however, the safety and efficacy of Erisine in treating infections due to these organisms have not been established in adequate and well-controlled trials: Gram-Positive Organisms: Alpha hemolytic streptococci (viridans group).
Gram-Negative Organisms: Moraxella (Branhamella) catarrhalis.
Other Microorganisms: Entamoeba histolytica, Treponema pallidum.
Disc Susceptibility Tests: Quantitative methods require measurement of zone diameters give the most precise estimates of antibiotic susceptibility. One recommended procedure uses Erisine class discs for testing susceptibility; interpretations correlate zone diameters of this disc test with MIC values for Erisine. With this procedure, a report from the laboratory of "susceptible" indicates the infecting organism is likely to respond to therapy. A report of "resistant" indicates the infective organism is not likely to respond to therapy. A report of "intermediate susceptibility" indicates the result be considered equivocal, and if, the pathogen is not fully susceptible to alternative clinically feasible drugs, the test should be repeated. This category provides a buffer zone, which prevents small, uncontrolled technical factors from causing major discrepancies in interpretation.
Note: Many strains of Haemophilus influenzae are resistant to Erisine alone, but are susceptible to Erisine and sulfonamides together. Staphylococci resistant to Erisine may emerge during a course of Erisine therapy. Culture and susceptibility testing should be performed.
How should I take Erisine?
Before applying Erisine, thoroughly wash the affected area with warm water and soap, rinse well, and pat dry. After washing or shaving, it is best to wait 30 minutes before applying the pledget (swab), topical gel, or topical liquid form. The alcohol in them may irritate freshly washed or shaved skin.
For patients using the pledget (swab), topical gel, or topical liquid form of Erisine:
Erisine will not cure your acne. However, to help keep your acne under control, keep using Erisine for the full time of treatment, even if your symptoms begin to clear up after a few days. You may have to continue using Erisine every day for months or even longer in some cases. If you stop using Erisine too soon, your symptoms may return. It is important that you do not miss any doses.
The dose of Erisine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of Erisine. If your dose is different, do not change it unless your doctor tells you to do so.
The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.
If you miss a dose of Erisine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.
Keep out of the reach of children.
Do not keep outdated medicine or medicine no longer needed.
Administration of drug is important to know because the drug absorption and action varies depending on the route and time of administration of the drug. A medicine is prescribed before meals or after meals or along with meals. The specific timing of the drug intake about food is to increase its absorption and thus its efficacy. Few work well when taken in empty stomach and few medications need to be taken 1 or 2 hrs after the meal. A drug can be in the form of a tablet, a capsule which is the oral route of administration and the same can be in IV form which is used in specific cases. Other forms of drug administration can be a suppository in anal route or an inhalation route.
Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.
You may take Erisine with or without food.
Do not crush, chew, break, or open an Erisine tablet or capsule. Swallow it whole.
Shake the oral suspension (liquid) well just before you measure a dose. Measure the liquid with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.
This medication can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using Erisine.
Take this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Erisine will not treat a viral infection such as the common cold or flu.
Store at room temperature away from moisture and heat, unless otherwise directed on the medicine label.
Pharmacokinetics of a drug can be defined as what body does to the drug after it is taken. The therapeutic result of the medicine depends upon the Pharmacokinetics of the drug. It deals with the time taken for the drug to be absorbed, metabolized, the process and chemical reactions involved in metabolism and about the excretion of the drug. All these factors are essential to deciding on the efficacy of the drug. Based on these pharmacokinetic principles, the ingredients, the Pharmaceutical company decides dose and route of administration. The concentration of the drug at the site of action which is proportional to therapeutic result inside the body depends on various pharmacokinetic reactions that occur in the body.
Orally administered Erisine ethylsuccinate suspensions and Filmtab tablets are readily and reliably absorbed. Comparable serum levels (Erisine ethylsuccinate) of Erisine are achieved in the fasting and nonfasting states.
Erisine diffuses readily into most body fluids. Only low concentrations are normally achieved in the spinal fluid, but passage of the drug across the blood-brain barrier increases in meningitis. In the presence of normal hepatic function, Erisine is concentrated in the liver and excreted in the bile; the effect of hepatic dysfunction on excretion of Erisine by the liver into the bile is not known. Less than 5 percent of the orally administered dose of Erisine is excreted in active form in the urine.
Erisine crosses the placental barrier, but fetal plasma levels (Erisine ethylsuccinate) are low. The drug is excreted in human milk.
Erisine acts by inhibition of protein synthesis by binding 50 S ribosomal subunits of susceptible organisms. It does not affect nucleic acid synthesis. Antagonism has been demonstrated in vitro between Erisine and clindamycin, lincomycin, and chloramphenicol.
Many strains of Haemophilus influenzae are resistant to Erisine alone but are susceptible to Erisine and sulfonamides used concomitantly.
Staphylocci resistant to Erisine may emerge during a course of therapy.
Erisine has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections as described in the INDICATIONS AND USAGE section.
Staphylococcus aureus(resistant organisms may emerge during treatment)
The following in vitro data are available, but their clinical significance is unknown.
Erisine exhibits in vitro minimal inhibitory concentrations (MIC's) of 0.5 μg/mL or less against most ( ≥ 90%) strains of the following microorganisms; however, the safety and effectiveness (Erisine ethylsuccinate) of Erisine in treating clinical infections due to these microorganisms have not been established in adequate and well controlled clinical trials.
Viridans group streptococci
Quantitative methods are used to determine antimicrobial minimum inhibitory concentrations (MIC's). These MIC's provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MIC's should be determined using a standardized procedure. Standardized procedures are based on a dilution methodrequires the use of standardized inoculum concentrations. This procedure uses paper disks impregnated with 15-μg Erisine to test the susceptibility of microorganisms to Erisine.
Reports from the laboratory providing results of the standard single-disk susceptibility test with a 15
ReviewsThe results of a survey conducted on ndrugs.com for Erisine are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Erisine. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.
Consumer reported administrationNo survey data has been collected yet
Information checked by Dr. Sachin Kumar, MD Pharmacology