Voorbeelden van het gebruik van Zoster in het Engels en hun vertalingen in het Nederlands
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Evaluation of Clinical Efficacy Afforded by ZOSTAVAX ZOSTAVAX significantly reduced the risk of developing zoster and PHN compared with placebo.
three times a day to lubricate zoster dipped in oil with a cotton swab.
ZOSTAVAX is a vaccine used to prevent shingles(zoster) and zoster-related post-herpetic neuralgia(PHN),
In subjects who developed zoster, ZOSTAVAX decreased the risk of subsequently developing PHN.
In the LTPS, there were 263 evaluable zoster cases reported among 261 patients 10.3/1000 person- years.
Overall, among vaccinated individuals who developed zoster, ZOSTAVAX significantly reduced overall acute and chronic zoster-associated pain compared with placebo.
In this study, herpes zoster reactivation was more common in patients treated with Vc+M+P compared with M+P 11% vs 3% respectively.
including serious cases of herpes zoster or hepatitis B virus(HBV) reactivation.
and herpes zoster- related post-herpetic neuralgia PHN.
which is thought to be the mechanism by which it protects against zoster and its complications See Immunogenicity.
is at risk for developing zoster.
Three(3%) of the 91 patients in the Vc+M+P treatment group who received prophylactic antivirals developed herpes zoster reactivation.
Of the 91 patients in the Vc+M+P treatment group who received prophylactic anti-virals developed herpes zoster reactivation.
which is necessary to lubricate zoster 6-7 times a day.
Reduction of zoster pain severity-by-duration in vaccinated individuals who developed zoster With regard to the acute pain(pain between 0-30 days)
In the vaccine group, the risk of developing PHN after zoster was 9%(27/315),
meningitis caused by herpes simplex or varicella zoster have been reported in multiple sclerosis patients receiving TYSABRI.
by patients who have had herpes zoster(shingles), and central neuropathic pain,
were followed for the development of zoster for a median of 3.1 years range 31 days to 4.9 years.
a booster dose to 201 zoster history-negative subjects 70 years of age or older who had received a first dose approximately 10 years previously as participants in the SPS, and(2) a first dose to 199 zoster history-negative subjects 70 years of age or older.