Examples of using Sovaldi in English and their translations into Dutch
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No drug-drug interaction data exists regarding the co-administration of Sovaldi with boceprevir or telaprevir.
Sovaldi in combination with ribavirin is recommended for 24 weeks in liver transplant recipients.
Sovaldi has mainly been studied in combination with ribavirin,
In particular, do not take Sovaldi if you are taking any of the following medicines.
The safety of Sovaldi has not been assessed in subjects with severe renal impairment eGFR.
Sovaldi was investigated in four main studies involving a total of 1305 patients infected with hepatitis.
The safety and efficacy of Sovaldi have not been established in patients with decompensated cirrhosis.
Consult the Summary of Product Characteristics for co-prescribed medicinal products before starting therapy with Sovaldi.
the active substance of Sovaldi, passes into human breast milk.
Sovaldi should always be taken in combination with other medicinal products for use against hepatitis C.
The safety of Sovaldi has not been assessed in patients with severe renal impairment or ESRD see section 4.4.
If you are sick(vomit) less than 2 hours after taking Sovaldi, take another tablet.
could result in loss of efficacy of Sovaldi see section 4.5.
The S282T substitution in NS5B was detected in a single subject receiving Sovaldi monotherapy in a Phase 2 study.
Sovaldi contains the active substance sofosbuvir which is given to treat hepatitis C virus infection in adults of 18 years and older.
And you notice within 18 hours of the time you usually take Sovaldi, you must take the tablet as soon as possible.
Sovaldi must be used in combination with other medicines used to treat chronic hepatitis C,
The clinical data to support the use of Sovaldi in patients with genotype 5 and 6 HCV infection is very
Sovaldi should only be co-administered with other direct-acting antiviral medicinal products if the benefit is considered to outweigh the risks based upon available data.
Sovaldi has not been studied in a Phase 3 study in treatment-experienced patients with genotype 1,