Pexeva is the most potent inhibitor of the reuptake of serotonin of all selective serotonin reuptake inhibitors (SSRIs) and has been studied in many randomised controlled trials (RCTs). However, these comparative studies provided contrasting findings and systematic reviews of RCTs have always considered the SSRIs as a group, and evidence applicable to this group of drugs might not be applicable to Pexeva alone. The present systematic review assessed the efficacy and tolerability profile of Pexeva in comparison with tricyclics (TCAs), SSRIs and newer or non‐conventional agents.
Other names for this medication:
Paroxetine,
Aropax,
Depaxil,
Deroxat,
Divarius,
Motivan,
Panex,
Parocen,
Parot,
Parox,
Paroxat,
Paroxetina,
Paxil,
Pexeva,
Sereupin,
Seroxat,
Xepar,
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Warfarin,
Spirolang,
Aplenzin,
Omeral,
Zepral,
Anagastra,
Purbac,
Rozex,
Alcinin,
Combutol,
Noroxin,
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Non-anastomotic strictures often result from ischemic and immunological events, occur earlier and are usually multiple and longer. The structure of 53BP1/H4-K20me2 complex uncovers a unique five-residue 53BP1 binding cage, remarkably conserved in the structure of Crb2, that best accommodates a dimethyllysine but excludes a trimethyllysine, thus explaining the methylation state-specific recognition of H4-K20. Using identical logistic models adjusted for age, baseline body mass index (BMI) and numerous covariates, the noracin information management abdominal-gain group and the peripheral-gain group were separately compared with 10,888 women who did not gain weight. Pharmacodynamics of the new beta blockader corgard (nadolol) in patients with stress-induced angina pectoris