Примери за използване на Develop a hypersensitivity reaction на Английски и техните преводи на Български
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About 5 in every 100 patients,who are treated with abacavir, develop a hypersensitivity reaction.
This patient did not develop a hypersensitivity reaction or injection site reaction. .
In clinical studies approximately 5% of subjects receiving abacavir develop a hypersensitivity reaction.
Patients taking Ziagen may develop a hypersensitivity reaction(serious allergic reaction) which can be life-threatening if treatment with Ziagen is continued.
Since Triumeq contains abacavir some patients taking Triumeq may develop a hypersensitivity reaction(serious allergic reaction). .
Anyone taking Kivexa could develop a hypersensitivity reaction to abacavir, which could be life threatening if they continue to take Kivexa.
In clinical studies approximately 5% of subjects receiving abacavir(which is also the active substance of Ziagen) develop a hypersensitivity reaction.
About 5 in every 100 patients,who are treated with Ziagen, develop a hypersensitivity reaction to the active ingredient abacavir.
Anyone taking Triumeq could develop a hypersensitivity reaction, which could be life threatening if they continue to take Triumeq.
Even patients who don't have the HLA-B*5701 gene may still develop a hypersensitivity reaction(a serious allergic reaction). .
Anyone taking Trizivir could develop a hypersensitivity reaction to abacavir, which could be life threatening if they continue to take Trizivir.
Since Trizivir contains abacavir(which is also the active substance of Ziagen)some patients taking Trizivir may develop a hypersensitivity reaction(serious allergic reaction) which can be life-threatening if you continue to take Trizivir.
Some people who take abacavir may develop a hypersensitivity reaction(a serious allergic reaction), which can be life-threatening if they continue to take abacavir containing products.
In populations similar to that enrolled in the PREDICT-1 study,it is estimated that 48% to 61% of patients with the HLA-B*5701 allele will develop a hypersensitivity reaction during the course of abacavir treatment compared with 0% to 4% of patients who do not have the HLA-B*5701 allele.
Even patients who don't have the HLAB*5701 gene may still develop a hypersensitivity reaction, described in this leaflet in the panel headed‘Hypersensitivity reactions'.
Even patients who don't have the HLA-B*5701 gene may still develop a hypersensitivity reaction(a serious allergic reaction), described in this leaflet in the panel headed‘Hypersensitivity reactions'.
Since Kivexa contains abacavir some patients taking Kivexa may develop a hypersensitivity reaction(serious allergic reaction) which can be life-threatening if treatment with Kivexa is continued.
Since Trizivir contains abacavir some patients taking Trizivir may develop a hypersensitivity reaction(serious allergic reaction) which can be life-threatening if treatment with Trizivir is continued.
Since Kivexa contains abacavir some patients taking Kivexa may develop a hypersensitivity reaction(serious allergic reaction) which can be life-threatening if you continue to take Kivexa.
In clinical studies,approximately 5% of subjects receiving abacavir developed a hypersensitivity reaction.
In clinical studies,approximately 5% of subjects receiving abacavir developed a hypersensitivity reaction.
If a patient develops a hypersensitivity reaction during the TORISEL infusion, despite the premedication, the infusion must be stopped and the patient observed for at least 30 to 60 minutes(depending on the severity of the reaction). .
About 3 to 4 in every 100 patients treated with abacavir in a clinical trial who did not have the HLAB*5701 gene developed a hypersensitivity reaction.
In clinical studies,approximately 5% of subjects receiving abacavir developed a hypersensitivity reaction; some of these were life-threatening and resulted in fatal outcome despite taking precautions.
Very rarely patients who have taken medicines containing abacavir in the past without any symptoms of hypersensitivity have developed a hypersensitivity reaction when they start taking these medicines again.
In one case of overdose the patient inadvertently received 7.6 mg of eribulin(approximately 4times the planned dose) and subsequently developed a hypersensitivity reaction(Grade 3) on Day 3 and neutropenia(Grade 3) on Day 7.
Patients who have previously experienced a hypersensitivity reaction to paclitaxel may be at risk to develop hypersensitivity reaction to docetaxel, including more severe hypersensitivity reaction. .
Patients who have previously experienced a hypersensitivity reaction to paclitaxel may be at risk to develop hypersensitivity reaction to docetaxel, including more severe hypersensitivity reaction. .
One patient in the 10 mg/kg<30kg group developed positive anti-tocilizumab antibodies without developing a hypersensitivity reaction and subsequently withdrew from the study.
If however, you suspect you are developing a hypersensitivity reaction contact your doctor immediately who will advise you whether you should stop taking Ziagen.