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1.
Southeast Asian J Trop Med Public Health ; 1993 Dec; 24(4): 672-6
Article in English | IMSEAR | ID: sea-34546

ABSTRACT

Two studies were conduct in Thailand in order to find appropriate falciparum malaria prophylactic drug regimens. The first study was done during June - September 1987 with 363 soldiers who received Fansimef (MSP) 1 tab/week (group 1), 337 soldiers who received MSP 1 tab/2 week (group 2) and 165 soldiers who received chloroquine 300 mg base weekly plus Fansidar 1 tab/week (group 3). At the end of the study there were 9 and 13 falciparum malaria episodes in groups 1 and 2, respectively, with incidence rates of 0.8 and 1.8 cases/100 person-months (P-M). In group 3, the corresponding values were 30 episodes and an incidence of 7.2/100 P-M. For the second study which lasted from October 1987 - January 1988 in the same area, 498 soldiers were given Fansimef 1/2 tab/week (group 4), 499 soldiers were given Lariam 1/2 tab/week (group 5) and 247 soldiers were given chloroquine plus Fansidar (group 6). Thirty malaria episodes were found in group 4, for an incidence of 2.0/100 P-M. In group 5, 23 episodes were found, for an incidence of 1.6/100 P-M. In group 6, 74 episodes occurred, ie an incidence of 12.2/100 P-M. The incidence rates of malaria among Fansimef 1 tab weekly, Fansimef half dose weekly or Lariam half dose weekly were not significantly different but were different from chloroquine plus Fansidar groups. Adverse events in each group were mild.


Subject(s)
Adult , Animals , Antibodies, Protozoan/isolation & purification , Blood/parasitology , Chloroquine/therapeutic use , Drug Combinations , Humans , Malaria, Falciparum/prevention & control , Male , Mefloquine/analogs & derivatives , Military Personnel , Plasmodium falciparum/immunology , Pyrimethamine/therapeutic use , Sulfadoxine/therapeutic use , Thailand
2.
Southeast Asian J Trop Med Public Health ; 1990 Dec; 21(4): 552-7
Article in English | IMSEAR | ID: sea-33273

ABSTRACT

Twenty eight adult male patients with acute uncomplicated falciparum malaria which showed RI or RII responses to quinine sulfate at the dosage of 600 mg 8 hourly for 7, 10 or 14 days were treated with a single dose of mefloquine (Lariam); 25 patients received 1000 mg, 2 received 750 mg and 1 received 500 mg. The initial response was good; there was no RII or RIII response. Three patients were lost to followup. Of 25 patients who stayed in the Bangkok Hospital for Tropical Diseases where there was no malaria transmission for 28-65 days, only one patient in the 1000 mg group had recrudescence on day 21. The cure rate was 96%. Our prospective study suggests that mefloquine was effective in the treatment of quinine resistant falciparum malaria and the risk of cross-resistance between quinine and mefloquine in P. falciparum in vivo is very low.


Subject(s)
Administration, Oral , Adolescent , Adult , Animals , Body Temperature/drug effects , Cross Reactions , Drug Resistance, Microbial , Humans , Malaria/blood , Male , Mefloquine/administration & dosage , Middle Aged , Plasmodium falciparum , Prospective Studies , Quinine/pharmacology
3.
Southeast Asian J Trop Med Public Health ; 1986 Mar; 17(1): 119-24
Article in English | IMSEAR | ID: sea-31495

ABSTRACT

Pharmacokinetic properties of ceftriaxone, such as sustained tissue drug levels over 24 hours after a single injection; good penetration of the antibiotic into cells; significant biliary excretion as active unchanged compound and high potency against S. typhi, should make it possible to significantly shorten the treatment of typhoid fever. To test this hypothesis a pilot, open study was initiated. 17 adult patients suffering from uncomplicated typhoid or paratyphoid fever, documented by blood culture, were treated with 4g ceftriaxone once daily for three days (4 patients) or two days (15 patients). The cure rate of 17 assessable patients was 94.2% (one failure). One possible relapse was observed two months after treatment. It is to be noted that no patient in the study suffered from a severe form of the disease.


Subject(s)
Adolescent , Adult , Aged , Ceftriaxone/blood , Female , Humans , Kinetics , Male , Middle Aged , Paratyphoid Fever/drug therapy , Salmonella paratyphi A , Salmonella paratyphi B , Typhoid Fever/drug therapy
4.
Southeast Asian J Trop Med Public Health ; 1978 Mar; 9(1): 74-8
Article in English | IMSEAR | ID: sea-35642

ABSTRACT

A total of 107 cases of trichomonas vaginitis were treated with different regimens of ornidazole. The overall success rate of the treatment assessed by wet smear and clinical signs after three days in 68 cases was 98.5%. The side effects were mild and of short duration. These were noted in 14.7% of the assessable cases. No significant differences were seen in the success rate between the three drug regimens and the preliminary conclusions of the trial are that ornidazole is safe and effective in the treatment of trichomonas vaginitis in Korean women with an oral dose of 1.0 gm, 1.0 gm plus 0.5 gm intravaginally or 2.0 gm given in a single day.


Subject(s)
Adult , Drug Administration Schedule , Female , Humans , Middle Aged , Nitroimidazoles/administration & dosage , Ornidazole/administration & dosage , Trichomonas Vaginitis/drug therapy
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