Примери за използване на Including stevens-johnson syndrome на Английски и техните преводи на Български
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Frequency not known exfoliative skin conditions including Stevens-Johnson syndrome.
Severe skin reactions, including Stevens-Johnson syndrome, have also been reported with Zebinix.
These reactions include anaphylaxis, angioedema, andexfoliative skin conditions including Stevens-Johnson syndrome.
Serious skin rash, including Stevens-Johnson syndrome, may develop in patients taking EVOTAZ.
Severe and life-threatening skin reactions have occurred in patients treated with nevirapine, including Stevens-Johnson syndrome(SJS) and toxic epidermal necrolysis(TEN).
Serious skin rash, including Stevens-Johnson syndrome, has been reported in patients taking atazanavir.
Erythema Rare rash with photosensitivity,severe skin reactions including Stevens-Johnson syndrome and toxic epidermal necrolysis.
Serious rash, including Stevens-Johnson Syndrome, Toxic Epidermal Necrolysis and Drug Rash with Eosinophilia and Systemic Symptoms.
Skin and subcutaneous tissue disorders Frequency not known:severe skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema multiforme and angioneurotic oedema.
During post-marketing experience the following additional side effects have been reported(frequency not known): hypersensitivity reactions including anaphylaxis, angioedema, rash, urticaria, andexfoliative skin conditions including Stevens-Johnson syndrome(see section 4.4).
Serious cutaneous reactions including Stevens-Johnson syndrome TEN and DRESS have been reported with the use of thalidomide therapy.
In view of the above, the PRAC considered that tetrazepam, compared to the medicines of the same pharmacological class,is associated with an increased risk of serious cutaneous adverse reactions including Stevens-Johnson syndrome, Toxic Epidermal Necrolysis, Erythema Multiform and DRESS syndrome which can be life threatening and fatal.
Serious skin rashes including Stevens-Johnson syndrome and toxic epidermal necrolysis have been reported in association with epoetin treatment.
Febuxostat treatment should be immediately stopped if serious allergic/hypersensitivity reactions, including Stevens-Johnson Syndrome, occur since early withdrawal is associated with a better prognosis.
Severe mucocutaneous reactions, including Stevens-Johnson Syndrome, some with fatal outcome, have been reported in association with Zevalin after pretreatment with rituximab.
During post-marketing experience of Janumet or sitagliptin, one of the active substances of Janumet, the following additional adverse reactions have been reported(frequency not known): hypersensitivity reactions including anaphylaxis, angioedema, rash, urticaria, andexfoliative skin conditions including Stevens-Johnson syndrome(see section 4.4).
Serious potentially life-threatening skin rashes, including Stevens-Johnson syndrome and toxic epidermal necrolysis(Lyell's Syndrome) have been reported.
Having assessed all available data on the risk of skin reactions, including post-marketing data in the EU and the published literature, the PRAC concluded that tetrazepam is associated with a low butincreased risk of serious skin reactions(including Stevens-Johnson syndrome, toxic epidermal necrolysis and DRESS syndrome) compared with other benzodiazepines.
There are angioedema andsevere skin reactions including Stevens-Johnson syndrome(SJS) and toxic epidermal necrolysis(TEN), which can cause patients die.
The PRAC considered, after having reviewed the available data that tetrazepam, compared to the medicines of the same pharmacological class,is associated with an increased risk of serious cutaneous adverse reactions including Stevens-Johnson syndrome, Toxic Epidermal Necrolysis, Erythema Multiform and Drug Reaction of Eosinophilia Systemic Symptoms(DRESS) which can be life threatening and fatal.
Severe cutaneous adverse reactions(SCARs), including Stevens-Johnson syndrome(SJS) and toxic epidermal necrolysis(TEN) have been reported in association with cemiplimab treatment(see section 4.4).
All the important safety information that has been included in the SmPC has been listed in order of importance: hypersensitivity reactions, infusion related reactions(Red Man Syndrome), severe bullous reactions(including Stevens-Johnson Syndrome(SJS) and toxic epidermal necrolysis(TEN)), warning concerning the possible adverse reactions with the higher loading dose of 12mg/kg bid.
Severe cutaneous adverse reactions(SCARs) including Stevens-Johnson syndrome(SJS) and toxic epidermal necrolysis(TEN), which can be life-threatening or fatal, have been reported see section.
Patients have rarely developed serious cutaneous reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis and erythema multiforme during treatment with VFEND.
Hypersensitivity reactions, including Stevens-Johnson syndrome, anaphylactic reactions, and angioedema are serious and are attributed to the alogliptin component of Incresync(see section 4.4).
Hypersensitivity reactions, including anaphylactic reactions, angioedema andexfoliative skin conditions including Stevens-Johnson syndrome and erythema multiforme have been observed for DPP-4 inhibitors and have been spontaneously reported for alogliptin in the post-marketing setting.
Severe cutaneous adverse reactions(SCARS), including Stevens-Johnson syndrome(SJS)/toxic epidermal necrolysis(TEN) and drug reaction with eosinophilia and systemic symptoms(DRESS) have been reported in post-marketing experience with Zebinix treatment(see section 4.4).
Rare serious hypersensitivity reactions to febuxostat, including Stevens-Johnson Syndrome, Toxic epidermal necrolysis and anaphylactic reaction/shock, have occurred in the postmarketing experience.
Severe cutaneous adverse reactions(SCARs), including Stevens-Johnson syndrome(SJS), toxic epidermal necrolysis(TEN) and drug reaction with eosinophilia and systemic symptoms(DRESS) have been reported with the use of EXJADE(see section 4.4).
If patient has developed allergic/hypersensitivity reactions including Stevens-Johnson Syndrome and acute anaphylactic reaction/shock, febuxostat must not be re-started in this patient at any time.