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Anxiety severe

Treatment- Primarily symptomatic and supportive maintain proper fluid and electrolyte balance and administer a tranquilizer to suppress anxiety. Severe withdrawal symptoms may require narcotic replacement. Gradual withdrawal using successively smaller doses will minimize symptoms. [Pg.887]

A 36-year-old woman with rapid-cycling bipolar II disorder and premenstrual mood exacerbation was treated as an out-patient with lamotrigine 400 mg/day, clonazepam 0.5 mg tds, and quetiapine 100 mg/day. She gained 9 kg in 6 months and was advised to reduce the dose of quetiapine to 50 mg/day. After 1 day, she reported nausea, dizziness, headache, and anxiety severe enough to preclude normal daily activities. She was instructed to take quetiapine 75 mg/day, but her symptoms continued and only resolved when she took 100 mg/day. Slower reduction in the dose of quetiapine (by 12.5 mg/day every 5 days) with an antiemetic, ondansetron, also failed. On a third attempt, prochlorperazine successfully reduced her withdrawal symptoms, although moderate nausea persisted for 2 days after complete withdrawal. [Pg.332]

Indications Psychoses involving hallucinations, agitation, manic phase of bipolar psychoses nausea and vomiting induced by CNS dysfunctions anxiety severe behavioral problems, abdominal pain associated with porphyria, delirium, neurogenic pain Common drug examples ... [Pg.5]

CifiHijClNj. White plates m.p. 125 C. Diazepam is one of several benzodiazepines which are very widely used as minor tranquillizers for allaying anxiety, as hypnotics or, in sufficiently high dosage given intravenously, as pre-anaesthetic sedatives. [Pg.132]

Anxiety is a normal reaction. Pathological anxiety interferes with daily-life activities and may be accompanied by autonomic symptoms (chest pain, dyspnoea and palpitations). Severe forms include phobic anxiety and panic disorder. [Pg.201]

Relcovaptan (SR-49059) is a selective, orally active V1aR antagonist that prevents pain of primary dysmenorrhea and inhibits preterm labour and could be useful in the treatment of Raynaud s phenomenon. The selective ViBR antagonist SSR149415 showed beneficial effects in the treatment of depression and anxiety in several animal models. [Pg.1277]

More than half of the patients receiving this drug by the parenteral route experience some adverse reaction. Severe and sometimes life-threatening reactions include leukopenia (low white blood cell count), hypoglycemia (low blood sugar), thrombocytopenia (low platelet count), and hypotension (low blood pressure). Moderate or less severe reactions include changes in some laboratory tests, such as the serum creatinine and liver function tests. Other adverse reactions include anxiety, headache, hypotension, chills, nausea, and anorexia Aerosol administration may result in fatigue a metallic taste in the mouth, shortness of breath, and anorexia... [Pg.103]

Promoting an Optimal Response to Therapy Treatment with a leprostatic drug may require many years. These patients are faced with long-term medical and drug therapy and possibly severe disfigurement. The nurse must spend time with these patients, allowing them to verbalize their anxieties, problems, and fears. [Pg.117]

The expected outcomes for the patient depend on the type and severity of the seizure but may include an optimal response to tiierapy (control of seizure), management of common adverse drug reactions (includes minimizing injury and maintaining normal oral mucous membranes), reduction in anxiety, and an understanding of and compliance with the prescribed therapeutic regimen. [Pg.259]

When severe anxiety is present, it is important to obtain the history from a family member or friend. During the time the history is taken, the nurse observes the patient for behavioral symptoms indicating anxiety (eg, psychomotor agitation [extreme restlessness], facial grimaces, tense posture). Physiologic manifestations of anxiety include increased blood... [Pg.277]

Antidepressant drugs are used to manage depressive episodes such as major depression or depression accompanied by anxiety. These drugs may be used in conjunction with psychotherapy in severe depression. The SSRIs also are used to treat obsessive-compulsive disorders. The uses of individual antidepressants are given in the Summary Drug Table Antidepressants. Treatment is usually continued for 9 months after recovery from the first major depressive episode. If the patient, at a later date, experiences another major depressive episode, treatment is continued for 5 years, and with a third episode, treatment is continued indefinitely. [Pg.282]

Verheul et al. (2004) pooled data from seven European acamprosate studies in an effort to identify patient-related predictors of response to the medication. Although they examined a number of potential predictors, including patients level of physiological dependence before treatment, family history of alcoholism, age of onset of alcoholism, baseline anxiety symptom severity, baseline craving, and gender, none was shown to interact with acamprosate treatment. These findings led the authors to conclude that, although the effect size for acamprosate was moderate, the medication can be considered potentially effective for all patients with alcohol dependence. [Pg.29]

Patients seen for flashbacks are treated with oral diazepam (15—30 mg/day for adults) if symptoms of anxiety are severe (Rumack 1987). Neuroleptics, especially haloperidol, have been implicated in a transient increase in visual flashbacks and are not recommended (Moskowitz 1971 Strassman 1984). Risperidone and selective serotonin reuptake inhibitors may also worsen symptoms of hallucinogen persisting perception disorder (Halpern and Pope 2003). The patient needs assurance of the self-limiting nature of the phenomenon and its decreasing frequency of reoccurrence with time. The patient should be reminded that any future use of hallucinogens or marijuana may precipitate similar symptoms (Strassman 1984). [Pg.223]

Death after the use of MDMA or MDEA is rare but may occur because of induction of cardiac arrhythmias or as a consequence of risk-taking behavior. Following its acute effects, MDMA may produce symptoms such as anxiety, depression, and confusion, which, in some cases, continue for several weeks (Dowling et al. 1987). [Pg.231]


See other pages where Anxiety severe is mentioned: [Pg.66]    [Pg.498]    [Pg.75]    [Pg.462]    [Pg.66]    [Pg.498]    [Pg.75]    [Pg.462]    [Pg.217]    [Pg.227]    [Pg.48]    [Pg.314]    [Pg.122]    [Pg.516]    [Pg.83]    [Pg.44]    [Pg.92]    [Pg.245]    [Pg.850]    [Pg.114]    [Pg.547]    [Pg.1124]    [Pg.1125]    [Pg.1222]    [Pg.1274]    [Pg.50]    [Pg.51]    [Pg.97]    [Pg.256]    [Pg.275]    [Pg.543]    [Pg.37]    [Pg.38]    [Pg.66]    [Pg.89]    [Pg.91]    [Pg.112]    [Pg.119]    [Pg.119]    [Pg.137]    [Pg.137]   
See also in sourсe #XX -- [ Pg.9 , Pg.32 , Pg.237 , Pg.256 ]




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