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1.
Clin Exp Dermatol ; 47(4): 735-738, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34609771

ABSTRACT

Patients who develop an immediate allergic reaction within the first 4 h of COVID-19 vaccine injection are recommended not to receive the same vaccine again. This recommendation mainly focuses on the mRNA and adenoviral vector COVID-19 vaccines, but data for whole virus vaccines are unknown. We report seven patients who developed an immediate reaction within 4 h (six had generalized urticaria, one had localized urticaria) after the first vaccination with CoronaVac, the inactivated SARS-CoV-2 vaccine. The results of skin tests and basophil activation tests suggested that spike peptides play a role in exacerbating urticaria in some patients. However, all subjects who developed urticaria within 4 h after CoronaVac vaccination were successfully revaccinated without graded challenge, although recurrent urticaria was common. This preliminary result indicates that acute urticaria alone should not be a contraindication for the second dose of CoronaVac if the supply of alternative vaccines is limited.


Subject(s)
COVID-19 , Urticaria , COVID-19/prevention & control , COVID-19 Vaccines/adverse effects , Contraindications , Humans , Immunization, Secondary , SARS-CoV-2 , Urticaria/etiology , Vaccination/adverse effects
2.
Int J Clin Pharmacol Ther ; 48(12): 803-13, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21084036

ABSTRACT

OBJECTIVES: To determine the efficacy of oxymetholone, an androgenic steroid, in combination with rHuEPO on hematologic and muscle mass in CAPD patients. METHODS: A double-blinded, placebo-controlled experimental study was conducted for 6 months and 24 CAPD patients were divided into two groups. The treatment group (n = 11) received rHuEPO plus oral oxymetholone (50 mg/tablet twice daily). The placebo group (n = 13) received rHuEPO plus a placebo twice daily. The evolution of the patients' hematologic parameters and the impact of the drugs on their muscle mass were evaluated. RESULTS: After 6 months of therapy, hematocrit and hemoglobin values of the treatment group were significantly different from those of the placebo group (38.1 ± 1.0% and 32.8 ± 0.9%, p = 0.001; 12.9 ± 0.3 g/dl and 11.0 ± 0.3 g/dl, p = 0.001 for hematocrit and hemoglobin, respectively). The increase in hematocrit and hemoglobin values observed in treatment group was statistically greater than those of the placebo group (p < 0.01). After 6 months, none of anthropometric parameters, albumin, protein or lean body mass levels, were significantly different from baseline in the placebo group. Conversely, most of the anthropometric parameters, albumin and lean body mass levels were significantly increased in the oxymetholone group (p < 0.05). The mean weight of subjects in the oxymetholone group changed from 63.82 ± 2.71 to 67.02 ± 3.26 kg (p = 0.001). The subjective global assessment score for 7 patients in the treatment group (63.6%) changed in a positive manner. A rise in liver enzymes was the main side effect observed in the treatment group. CONCLUSIONS: Oxymetholone significantly enhances the erythropoietic effects of rHuEPO and improves the nutritional status of CAPD patients. However, significant increases in liver enzymes need to be monitored closely.


Subject(s)
Anemia/drug therapy , Erythropoietin/administration & dosage , Muscle, Skeletal/drug effects , Oxymetholone/administration & dosage , Peritoneal Dialysis, Continuous Ambulatory , Adult , Aged , Body Composition , Double-Blind Method , Drug Therapy, Combination , Erythropoietin/adverse effects , Female , Hemoglobins/analysis , Humans , Liver/drug effects , Male , Middle Aged , Nutritional Status , Oxymetholone/adverse effects , Recombinant Proteins , Serum Albumin/analysis
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