Примери за използване на Risk of respiratory depression на Английски и техните преводи на Български
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Patients should be monitored closely for the potential risk of respiratory depression.
The risk of respiratory depression is less in patients receiving chronic opioid therapy as these patients will develop tolerance to respiratory depressant effects.
Patients without maintenance opioid therapy(see section 4.1)as there is an increased risk of respiratory depression.
Given the possibility of increasing the risk of respiratory depression, the concomitant use of benzodiazepines and sodium oxybate should be avoided.
The use of concomitant central nervous system depressants may increase the risk of respiratory depression(see section 4.5).
Due to the risk of respiratory depression, ABSTRAL is contraindicated in the management of acute or postoperative pain including headache/migraine and in opioid non-tolerant patients.
A lower dose is recommended for patients with chronic respiratory failure due to the risk of respiratory depression.
Benzodiazepines Given the possibility of increasing the risk of respiratory depression, the concomitant use of benzodiazepines and Xyrem should be avoided.
Particular care is required in patients with chronic respiratory insufficiency due to the risk of respiratory depression.
This section also contains other warnings,including warnings about the risk of respiratory depression, dependence and potential for abuse, and use in children and elderly patients.
A lower dose is also recommended for patients with chronic respiratory insufficiency due to the risk of respiratory depression.
However, in these cases,try not to use narcotic painkillers because of the increased risk of respiratory depression in a preterm child more sensitive to these drugs(compared with the born on time).
The combined use of alcohol, or any CNS-depressant medicinal product,with sodium oxybate may result in potentiation of the CNS-depressant effects of sodium oxybate as well as increased risk of respiratory depression.
Initiation of treatment with methadone presents a potential risk of respiratory depression and should be undertaken with care.
Codeine-containing medicines should only be used to treat acute(short lived) moderate pain in children above 12 years of age, andonly if it cannot be relieved by other painkillers such as paracetamol or ibuprofen, because of the risk of respiratory depression associated with codeine use.
Respiration should be monitored in non-intubated patients due to the risk of respiratory depression and in some case apnoea(see section 4.8).
The use of concomitant CNS-active medicinal products may increase the risk of respiratory depression(see section 4.5).
Dexmedetomidine is notable for its ability to provide sedation without risk of respiratory depression(unlike other commonly used sedatives such as propofol, fentanyl, and midazolam) and can provide cooperative or semi-arousable sedation.
The use of concomitant central nervous system depressants may increase the risk of respiratory depression(see section 4.5).
The use of concomitant CNS-active medicinal products may increase the risk of respiratory depression(see section 4.5).
This medication should not be used in conjunction with alcohol or any other central nervous system(CNS) depressant due to the risk of respiratory depression and other significant CNS depressant effects.
Patients with pain who receive chronic opioid therapy develop tolerance to respiratory depression and hence the risk of respiratory depression in these patients is reduced.
Patients with pain who receive chronic opioid therapy develop tolerance to respiratory depression and hence the risk of respiratory depression in these patients may be reduced.
The minimum dosing interval of one sublingual tablet per hour, in order toprevent/ minimise the important identified risk of respiratory depression and the important potential risk of overdose;
Due to the long half-life of buprenorphine,neonatal monitoring for several days after birth should be considered to prevent the risk of respiratory depression or withdrawal syndrome in neonates.
Due to the long half-life of buprenorphine, neonatal monitoring for several days should be considered atthe end of pregnancy, to prevent the risk of respiratory depression or withdrawal syndrome in neonates.
Due to the long half-life of buprenorphine, neonatal monitoring for several days should be considered atthe end of pregnancy, to prevent the risk of respiratory depression or withdrawal syndrome in neonates.
Opioid-naïve patients because of the risk of life-threatening respiratory depression.
Increasing the risk of extreme sedation and respiratory depression from these agents.
Thereby, increasing the risk of extreme sedation and respiratory depression from these agents.