Примери за използване на Serious adverse reaction на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
No serious adverse reaction was reported.
The most commonly reported serious adverse reaction was cellulitis(1.1%).
Bial claimed that the drug was given to 108 patients“without any moderate or serious adverse reaction.”.
The most common serious adverse reaction was epistaxis.
Bial says that the new drug had already been administered to 108 patients"without any moderate or serious adverse reaction.".
The most important serious adverse reaction is hypertension.
Throughout this trial,the new drug had already been administered to 108 patients without any moderate or serious adverse reaction.”.
The most commonly reported serious adverse reaction was pneumonia(11.5%).
Bial pharmaceutical said in statement that throughout this trial,the new drug had already been administered to 108 patients“without any moderate or serious adverse reaction.”.
The only serious adverse reaction occurring in> 2% of patients was anaemia(5%).
That Member State shall report the suspected unexpected serious adverse reaction in accordance with paragraph 1 of this Article.
Neutropenia as a serious adverse reaction occurred in 29% of the patients and febrile neutropenia occurred in 3% of the patients.
When treatment is given at home, support from another responsible person should be available for treating adverse reactions orto summon help should a serious adverse reaction occur.
There was no evidence for serious adverse reaction caused by imiquimod in paediatric patients.
The competent authority or authorities shall organise inspections andcarry out control measures as appropriate whenever there is any serious adverse reaction or serious adverse event.
Any term that includes at least one serious adverse reaction is identified with a dagger(†).
If a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified or discontinued, if appropriate, until the adverse reaction abates or decreases in severity.
The most frequently reported treatment-associated serious adverse reaction(SAR) was dehydration(4%), experienced by 5 patients.
If a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified or discontinued, if appropriate, until the adverse reaction abates or decreases in severity.
INN should be discontinued immediately at the first signs or symptoms of any serious adverse reaction and patients should be advised to contact their prescriber for advice.
The most common serious adverse reaction reported with Zavesca treatment in clinical studies was peripheral neuropathy(see section 4.4).
Delafloxacin should be discontinued immediately at the first signs or symptoms of any serious adverse reaction and patients should be advised to contact their prescriber for advice.
The most important serious adverse reaction was hepatocellular injury, observed in two patients(< 1%).
You should not take fluoroquinolone/quinolone antibacterial medicines, including[product name],if you have experienced any serious adverse reaction in the past when taking a quinolone or fluoroquinolone.
The most frequently reported serious adverse reaction was immune reconstitution syndrome and rash.
Acute pancreatitis is a serious adverse reaction and is attributed to the alogliptin component of Incresync(see section 4.4).
If sofosbuvir is used in combination with peginterferon alfa, anda patient has a serious adverse reaction potentially related to this drug, the peginterferon alfa dose should be reduced or discontinued.
Corporal rupture was reported as a serious adverse reaction after Xiapex injection in 5 out of 1044 patients(0.5%) in the controlled and uncontrolled clinical trials in Peyronie's disease.
A greater percentage of abatacept- than placebo treated patients with COPD developed a serious adverse reaction(5.4% vs. 0%), including COPDexacerbation(1 of 37 patients[2.7%]) and bronchitis(1 of 37 patients[2.7%]).
In one additional patient, a serious adverse reaction of infusion related reaction was reported(0.3%).