Примери за използване на Cocs на Английски и техните преводи на Български
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Therapeutic effects of COCs.
Can a woman safely take COCs throughout her life?
During this period, the possibility of conception is also minimal,as in the normal use of COCs.
The connection with the use of COCs is not proven.
Indeed, the side effects of COCs exist, in principle, as they have any other medicines.
It started being used in COCs in 1964.
With the use of higher dosed COCs(50 microgram ethinyl estradiol) the risk of endometrial and ovarian cancer is reduced.
A causal relationship with the use of COCs is not known.
If you have been taking COCs containing 21 pills, then a new stack to begin no later than the day after the seven-day break.
There is no consensus as to whether the occurrence of these events is associated with the use of COCs.
The safety profile of EE/DRSP- COCs in the approved indication is well known.
Women with a tendency to chloasma should avoid exposure to the sun orultraviolet radiation whilst taking COCs.
The known greater risk of venous thromboembolic events(VTE)for DRSP-COCs in comparison with levonorgestrel(LNG)-COCs;
Women with hypertriglyceridaemia, or a family history thereof,may be at an increased risk of pancreatitis when using COCs.
It is better to take care of everything in advance andstart drinking COCs at least one cycle before the alleged menstruation.
It is proved that treatment with antibiotics or anticonvulsants, and diarrhea, which lasts several days,reduces the contraceptive effect of COCs.
It is better to take care of everything in advance andstart drinking COCs at least one cycle before the alleged menstruation.
A meta-analysis of 54 epidemiological studies reported that there is aslightly increased risk(RR= 1.24) of having breast cancer diagnosed in women who are currently using COCs.
It is known and described in the SmPCs of all COCs that postponing a withdrawal bleed will introduce higher risk of intracyclic bleeding in most women.
The observed pattern of increased risk may be due to an earlier diagnosis of breast cancer in COC users,the biological effects of COCs or a combination of both.
Epidemiological studies have suggested an association between the use of COCs in general and an increased risk of arterial thrombotic and thromboembolic diseases such as myocardial infarction, and of cerebrovascular accidents.
The observed pattern of increased risk may be due to an earlier diagnosis of breast cancer in COC users,the biological effects of COCs or a combination of both.
The efficacy of COCs may be reduced in the event of e.g., missed tablets(see section 4.2), gastrointestinal disturbances during active tablet-taking(see section 4.2) or use of concomitant medicinal.
Recurrence of cholestatic jaundice which occurred first during pregnancy orprevious use of sex steroids necessitates the discontinuation of COCs.
Although COCs may have an effect on peripheral insulin resistance and glucose tolerance, there is no evidence for a need to alter the therapeutic regimen in diabetics using low-dose COCs(containing 0.05 mg ethinylestradiol).
Therefore, a hepatic tumour should be considered in the differential diagnosis whensevere upper abdominal pain, liver enlargement or signs of intra-abdominal haemorrhage occur in women taking COCs.
More recent studies assessing the VTE risk in users of various COCs and CPA/EE(including Lidegaard 2009, Hylckama 2009) had major methodological flaws(missing data for confounders) that raise questions about the validity of their conclusions.
Furthermore, concomitant use of another hormonal contraceptive being reported as an additional suspected drug was documented in 21(2.2%) of received TE cases;20 patients received concomitantly various COCs and one case reported concomitant intrauterine device(IUD)(levonorgestrel-releasing intrauterine system) use.
The efficacy of COCs may be reduced in the event of e.g., missed tablets(see section 4.2), gastro-intestinal disturbances during active tablet-taking(see section 4.2) or use of concomitant medicinal products that decrease the plasma concentrations of nomegestrol acetate and/or estradiol(see section 4.5).
Overall the risk of VTE in usersof low oestrogen dose(< 50 µg ethinyloestradiol) COCs is two to threefold higher than for non-users of COCs who are not pregnant and remains lower than the risk associated with pregnancy and delivery.