Generic Name: Super avana
What is Super Avana?
It keeps bacteria from growing by stopping their production of proteins early in their life cycle, while other antibiotics intervene later in the process. The most frequently reported side effects attributed to Zyvox in clinical studies were headache 6.
The most important laboratory test change was a decrease in platelet counts. Zyvox may interact with certain other drugs, including over-the-counter cold remedies that contain pseudoephedrine or phenylpropanolamine, and cause an increase in blood pressure.
The drug's manufacturer, Pharmacia and Upjohn, expects Zyvox to be used mainly in hospitals or long-term care facilities, to lessen the chance that inappropriate use of the antibiotic would lead to an increase in resistant organisms.
And since this is the only drug that works against certain bugs, resistance to this drug would be a serious problem," explains Clark. YOU MAY ALSO LIKE.
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How should I take Super Avana?
Specific Populations Geriatric Patients The pharmacokinetics of linezolid are not significantly altered in elderly patients 65 years or older. Pediatric Patients The pharmacokinetics of linezolid following a single intravenous dose were investigated in pediatric patients ranging in age from birth through 17 years including premature and full-term neonatesin healthy adolescent subjects ranging in age from 12 through 17 years, and in pediatric patients ranging in age from 1 week through 12 years.
Drug Interactions Drugs Metabolized by Cytochrome P450 Linezolid is not an inducer of cytochrome P450 CYP450 in rats. Antibiotics Aztreonam: The pharmacokinetics of linezolid or aztreonam are not altered when administered together. Antioxidants The potential for drug-drug interactions with linezolid and the antioxidants Vitamin C and Vitamin E was studied in healthy volunteers.
What should I avoid while taking Super Avana?
ZYVOX was studied for the treatment of community-acquired CAP and hospital-acquired HAP pneumonia due to MDRSP by pooling clinical data from seven comparative and non-comparative Phase 2 and Phase 3 studies involving adult and pediatric patients. The pooled MITT population consisted of all patients with S. Adult patients with clinically documented complicated skin and skin structure infections were enrolled in a randomized, multi-center, double-blind, double-dummy trial comparing study medications administered IV followed by medications given orally for a total of 10 to 21 days of treatment.
There were 400 linezolid-treated and 419 oxacillin-treated patients enrolled in the study. A modified intent-to-treat MITT analysis of 316 linezolid-treated patients and 313 oxacillin-treated patients included subjects who met all criteria for study entry. The cure rates by pathogen for microbiologically evaluable patients are presented in Table 18.
A separate study provided additional experience with the use of ZYVOX in the treatment of methicillin-resistant Staphylococcus aureus MRSA infections.
Super Avana side effects
However, because the mean half life of linezolid is not significantly different in males and females, plasma concentrations in females are not expected to substantially rise above those known to be well tolerated and, therefore, dose adjustments are not required. In sexually mature animals these effects were reversible. However, these effects did not reverse in juvenile animals treated with linezolid for nearly the entire period of sexual maturation. Abnormal sperm morphology in testis of adult male rats, and epithelial cell hypertrophy and hyperplasia in the epididymis were noted.
Linezolid appeared to affect the maturation of rat spermatozoa. Supplementation of testosterone had no effect on linezolid-mediated fertility effects.
Common Super Avana ide effects may include:
The decision could also set a precedent that facilitates full registration by the MCC of a generic linezolid product.
Doses of Linezolid are usually administered every 12 hours.
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Therefore, linezolid has the potential for interaction with adrenergic and serotonergic agents.
In each arm 37 patients with Gram-positive infections died. At baseline 34 patients in the linezolid arm and 32 patients in the comparator arm had Gram-negative bacteremia. An additional 28 patients in the linezolid arm and 17 patients in the comparator arm developed Gram-negative bacteremia during treatment.
Linezolid is approved for the treatment of vancomycin-resistant Enterococcus faecium infections, nosocomial pneumonia, community-acquired pneumonia, uncomplicated skin and skin structure infections, and complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis. Linezolid is not approved for the treatment of catheter-related bloodstream infections, catheter-site infections, or for the treatment of infections caused by Gram-negative bacteria.
Where can I get more information?
Should superinfection occur during therapy, appropriate measures should be taken.
When used solely for the prevention of postmenopausal osteoporosis, alternative treatments should be carefully considered.