Safety evaluation of SPF66 malaria vaccine in Brazil

The frequency and description of side effects secondaiy to the subcutaneous application of SPf66 malaria vaccine and placebo are reported for each dose of application in the participants of the vaccine efficacy trial in Brazil. Side effects evaluated two hours after each application were detected in...

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Main Authors: LM. Urdaneta, A. Prata, C.J. Struchiner, C.E. Tosta, P. Tauil, M. Boulos
Format: Article
Language:English
Published: Sociedade Brasileira de Medicina Tropical (SBMT) 1996-10-01
Series:Revista da Sociedade Brasileira de Medicina Tropical
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86821996000500014&lng=en&tlng=en
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spelling doaj-f5148adcf8184b18a10e3572c5d014532020-11-25T00:35:30ZengSociedade Brasileira de Medicina Tropical (SBMT)Revista da Sociedade Brasileira de Medicina Tropical1678-98491996-10-0129549750110.1590/S0037-86821996000500014S0037-86821996000500014Safety evaluation of SPF66 malaria vaccine in BrazilLM. UrdanetaA. PrataC.J. StruchinerC.E. TostaP. TauilM. BoulosThe frequency and description of side effects secondaiy to the subcutaneous application of SPf66 malaria vaccine and placebo are reported for each dose of application in the participants of the vaccine efficacy trial in Brazil. Side effects evaluated two hours after each application were detected in 8.0%, 30.2% and 8.8%, for the Is', and 3"' dose, respectively, in the SPf66group, and in 7.0%, 8.5% and 2.9% in the placebo group. Local reactions such as mild inflammation, nodule and pain or erythema frequently accompanied by pruritus were the most common reactions detected in both groups (3-8%, 29.1% and 8.5% in the SPf66 group and 4.0%, 7.6% and 2.5% in the placebo group). Among vaccinees, local side effects after the 2nd dose were more frequent in females. Systemic side effects were expressed mainly through general symptoms referred by the participants and were most frequent after the 1st dose in both groups (4.3% in the SPf66 group and 3-0% in the placebo group). Muscle aches and fever were refewred by few participants. No severe adverse reactions were detected for either dose of application or group.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86821996000500014&lng=en&tlng=enVacina antimalãricaSegurança SPf66Ensaio de campo SPf66
collection DOAJ
language English
format Article
sources DOAJ
author LM. Urdaneta
A. Prata
C.J. Struchiner
C.E. Tosta
P. Tauil
M. Boulos
spellingShingle LM. Urdaneta
A. Prata
C.J. Struchiner
C.E. Tosta
P. Tauil
M. Boulos
Safety evaluation of SPF66 malaria vaccine in Brazil
Revista da Sociedade Brasileira de Medicina Tropical
Vacina antimalãrica
Segurança SPf66
Ensaio de campo SPf66
author_facet LM. Urdaneta
A. Prata
C.J. Struchiner
C.E. Tosta
P. Tauil
M. Boulos
author_sort LM. Urdaneta
title Safety evaluation of SPF66 malaria vaccine in Brazil
title_short Safety evaluation of SPF66 malaria vaccine in Brazil
title_full Safety evaluation of SPF66 malaria vaccine in Brazil
title_fullStr Safety evaluation of SPF66 malaria vaccine in Brazil
title_full_unstemmed Safety evaluation of SPF66 malaria vaccine in Brazil
title_sort safety evaluation of spf66 malaria vaccine in brazil
publisher Sociedade Brasileira de Medicina Tropical (SBMT)
series Revista da Sociedade Brasileira de Medicina Tropical
issn 1678-9849
publishDate 1996-10-01
description The frequency and description of side effects secondaiy to the subcutaneous application of SPf66 malaria vaccine and placebo are reported for each dose of application in the participants of the vaccine efficacy trial in Brazil. Side effects evaluated two hours after each application were detected in 8.0%, 30.2% and 8.8%, for the Is', and 3"' dose, respectively, in the SPf66group, and in 7.0%, 8.5% and 2.9% in the placebo group. Local reactions such as mild inflammation, nodule and pain or erythema frequently accompanied by pruritus were the most common reactions detected in both groups (3-8%, 29.1% and 8.5% in the SPf66 group and 4.0%, 7.6% and 2.5% in the placebo group). Among vaccinees, local side effects after the 2nd dose were more frequent in females. Systemic side effects were expressed mainly through general symptoms referred by the participants and were most frequent after the 1st dose in both groups (4.3% in the SPf66 group and 3-0% in the placebo group). Muscle aches and fever were refewred by few participants. No severe adverse reactions were detected for either dose of application or group.
topic Vacina antimalãrica
Segurança SPf66
Ensaio de campo SPf66
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86821996000500014&lng=en&tlng=en
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