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Side effects risks

SUI. Systemic estrogen therapy also carries numerous short- and long-term side effect risks (mastodynia, uterine bleeding, nausea, thromboembolism, cardiac and cerebrovascular ischemic events, and enhanced breast and endometrial cancer risks). If estrogens are to be used in SUI management, only locally-administered products should be used (Table 50-4). [Pg.811]

EPS, extra pyramidal side effects. Relative side-effect risk , negligible +, low ++, moderate +++, moderately high ++++, high. °Side effects shown are relative risk based on doses within the recommended therapeutic range, individual patient risk varies depending on patient-specific factors. [Pg.819]

Factors That Affect Compliance Side Effects, Risk-Benefit Ratio, Drug-Drug Interactions, Pharmacokinetic or Pharmacodynamic Effects, Cost, and Preferences... [Pg.325]

NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS RIBAVIRIN 1. t side-effects, risk of lactic acidosis, peripheral neuropathy, pancreatitis, hepatic decompensation, mitochondrial toxicity and anaemia with didanosine and stavudine 2.1 efficacy of lamivudine 1. Additive side-effects t intracellular activation of didanosine and stavudine 2. J intracellular activation of lamivudine 1. Not recommended. Use with extreme caution monitor lactate, LFTs and amylase closely. Stop co-administration if peripheral neuropathy occurs. Stavudine and didanosine carry a higher risk 2. Monitor HIV RNA levels if they T, review treatment combination... [Pg.608]

Pharmacotherapy algorithms should emphasize monotherapies with antipsychotics of optimal efficacyiside-effect ratios and progress to medications with greater side-effect risks and to combination regimens in treatment-resistant patients. [Pg.1209]

Selective serotonin reuptake inhibitors (SSRIs) are the first-line therapy for PTSD. Efficacy for fluoxetine, paroxetine, and sertraline has been demonstrated in well-designed double-blind placebo-controlled studies to reduce all symptom domains (intrusive recollection, avoidance/numbness, and hyperarousal). - Other treatment options include the tricyclic antidepressants (TCAs) amitriptyline and imipramine and the irreversible monoamine oxidase inhibitor (MAOl) phenelzine, which have been shown to reduce re-experiencing. However, in comparison with SSRIs, TCAs and phenelzine are associated with a higher incidence of side-effects, risk of overdose, and poor compliance. Alprazolam has demonstrated anecdotal efficacy however, regular use of benzodiazepines is not recommended. Benzodiazepines can be used on an as-needed basis for specific symptoms (e.g. sleep disturbances). CBT has shown beneficial effects in relatively well-controlled studies, while the results with exposure therapy are... [Pg.231]

It s best to take SAMe with vitamins Bs, B, folic acid, magnesium, and calcium. These help it work better and reduce any side-effect risks. Because this supplement is highly unstable, buy it in the form of enteric-coated tablets stored in foil packets and keep the pills in the foil until just before you take them. [Pg.86]

Innovation offered advice sessions/customer reports (tax, expenses, drug consumption/side effects, risks, health), remote access, peripheral services, health management 3. Innovation information, newfields, services/ support /follow-ups, hazards, evaluations... [Pg.100]

The maximum daily dose of naproxen is 1500 mg/ day and is the point where increased doses are no longer efficacious and produce significant side-effect risks. [Pg.224]


See other pages where Side effects risks is mentioned: [Pg.438]    [Pg.157]    [Pg.77]    [Pg.243]    [Pg.212]    [Pg.323]    [Pg.140]    [Pg.101]    [Pg.34]    [Pg.132]    [Pg.124]    [Pg.503]    [Pg.1221]    [Pg.131]    [Pg.476]   


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