Apotex corp zolpidem

Zolpidem tartrate tablets, USP have been shown to decrease sleep latency for up to 35 days in controlled clinical studies [see Clinical Corp 14 ]. The clinical trials performed in support of efficacy were 4 to 5 weeks in duration with apotex final formal assessments of sleep latency performed zolpidem the end of treatment.

Prescription Drug Information: Zolpidem Tartrate (Page 4 of 5)

The recommended initial dose is 5 mg for women and either 5 or 10 apotex for men, apotex corp zolpidem, taken only once per night zolpidem before bedtime with at least 7 to 8 hours corp before the planned time of awakening.

If the corp mg dose is not effective, the dose can be increased to 10 mg. In some patients, the higher morning blood levels apotex use of the 10 mg dose increase the risk of next day impairment of driving and other activities that require full alertness [see Warnings zolpidem Precautions 5.

apotex corp zolpidem

The total dose of zolpidem tartrate tablets should not exceed 10 mg once daily immediately before bedtime. The recommended initial doses for women and men are different because zolpidem clearance is lower in women, apotex corp zolpidem.

Patients with hepatic insufficiency do not clear the drug as rapidly as normal subjects.

Drugs@FDA: FDA Approved Drug Products

The recommended dose of zolpidem tartrate tablets in both of these patient populations is 5 mg once daily immediately before bedtime [see Warnings and Precautions 5. Viagra ägypten preis corp not scored.

Observed reactions include anaphylaxis and angioedema [see Warnings and Precautions 5, apotex corp zolpidem. Co-administration with other CNS depressants e. Dosage adjustments of zolpidem and of other concomitant CNS depressants may be necessary when zolpidem is administered with such agents because of the potentially additive effects. Apotex use of zolpidem with other sedative-hypnotics including other zolpidem products at bedtime or the middle of the night is not recommended [see Dosage and Administration 2.

Zolpidem risk of next-day psychomotor dapsone 300mg, including impaired driving, is increased if zolpidem is taken with less than a full night corp sleep remaining 7 to 8 hours ; if a higher than the recommended dose is taken; if co-administered with other CNS depressants; or if co-administered with other drugs that increase the blood levels of zolpidem.

Patients should be cautioned against driving and other activities requiring complete mental alertness if zolpidem is taken in these circumstances [see Apotex and Administration 2 and Clinical Studies Worsening of insomnia or the emergence of new thinking or behavior abnormalities may be the consequence of an unrecognized psychiatric or physical disorder, apotex corp zolpidem. Some patients have had additional symptoms such as dyspnea, throat closing or nausea and vomiting that suggest anaphylaxis.

Some zolpidem have required medical therapy in the emergency department. If angioedema involves the throat, glottis or larynx, airway obstruction may occur and be fatal.

Zolpidem Tartrate

Patients who develop angioedema after treatment with zolpidem should not be rechallenged corp the drug. Some of these changes included decreased inhibition e. Visual and auditory hallucinations have been reported. Other complex behaviors e. Amnesia, anxiety and zolpidem neuro-psychiatric symptoms may also occur, apotex corp zolpidem. It can rarely be determined with certainty whether a particular instance of the abnormal behaviors listed above is drug induced, spontaneous in origin, or a result of apotex underlying psychiatric or physical disorder.

Nonetheless, apotex corp zolpidem, the emergence of any new behavioral sign or symptom of concern requires careful and immediate evaluation.

APO-Zolpidem

Suicidal zolpidem may corp present in such patients and protective measures may be required. Intentional overdosage is more apotex in this group of patients; therefore, the lowest number of tablets that is feasible should be prescribed for the patient at any one time, apotex corp zolpidem. Share this Drug Information.

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