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restoril 30 mg temazepam buy restoril

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Description

restoril 30 mg temazepam

restoril 30 mg temazepam Capsules USP, 7.5 mg, 15 mg, 22.5 mg, and 30 mg, are for
oral administration.

7.5 mg, 15 mg, 22.5 mg, and 30 mg Capsules Active Ingredient: temazepam USP

Classification

Therapeutic: sedative/hypnotics
Pharmacologic: benzodiazepines
Schedule IV
Pregnancy Category X

drescription restoril 30 mg

7.5 mg Capsules

Inactive Ingredients: FD&C Blue #1, FD&C Red #3, gelatin, lactose, magnesium stearate, red iron oxide, titanium dioxide. May also include: n-butyl alcohol, iron oxide red, shellac, shellac glaze, SD-35A alcohol.

15 mg Capsules

Inactive Ingredients: FD&C Blue #1, FD&C Red #3, gelatin, lactose, magnesium stearate, red iron oxide, titanium dioxide. May also include: n-butyl alcohol, FD&C Blue #1/Brilliant Blue FCF Aluminum Lake, iron oxide red, isopropyl alcohol, propylene glycol, shellac, shellac glaze, SD-35A alcohol, SD-45 alcohol.

22.5 mg Capsules

Inactive Ingredients: FD&C Blue #1, FD&C Red #3, gelatin, lactose, magnesium stearate, red iron oxide, titanium dioxide. May also include: n-butyl alcohol, FD&C Blue #1/Brilliant Blue FCF Aluminum Lake, iron oxide red, isopropyl alcohol, propylene glycol, shellac, shellac glaze, SD-35A alcohol, SD-45 alcohol.

30 mg Capsules

Inactive Ingredients: FD&C Blue #1, FD&C Red #3, gelatin, lactose, magnesium stearate, red iron oxide, titanium dioxide. May also include: n-butyl alcohol, FD&C Blue #1/Brilliant Blue FCF Aluminum Lake, iron oxide red, isopropyl alcohol, propylene glycol, shellac, shellac glaze, SD-35A alcohol,
SD-45 alcohol.

Geriatric Use

Clinical studies of Restoril did not include sufficient numbers of subjects aged 65 and over to
determine whether they respond differently from younger subjects. Other reported clinical
experience has not identified differences in response between the elderly and younger patients.
In general, dose selection for an elderly patient should be cautious, usually starting at the low end
of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac
function, and of concomitant disease or other drug therapy commonly observed in this
population. Restoril 7.5 mg is recommended as the initial dosage for patients aged 65 and over
since the risk of the development of oversedation, dizziness, confusion, ataxia and/or falls
increases substantially with larger doses of benzodiazepines in elderly and debilitated patients.

How should I store restoril 30 mg ?

Store RESTORIL between 68°F to 77°F (20°C to 25°C).
Keep RESTORIL and all medicines out of the reach of children.

What should I avoid while taking restoril 30 mg?

Do not drive, operate machinery, do other dangerous activities or do anything that needs you to be alert until you know how restoril 30 mg affects you.
You should not drink alcohol while you are taking restoril 30 mg.

How should I take restoril 30 mg?

See “What is the most important information I should know about restoril 30 mg?”
Take RESTORIL exactly as your healthcare providers tell you to take it. Take restoril 30 mg right before you get into bed.
Do not take restoril 30 mg unless you are able to get a full night’s sleep before you must be active again.
If you take too much restoril 30 mg or overdose, get emergency treatment right away.

Adverse Reactions/Side Effects restoril 30 mg

CNS: abnormal thinking, behavior changes, hangover, dizziness, drowsiness, hallucinations, lethargy, paradoxic excitation, sleep— driving. EENT: blurred vision.
GI: constipation, diarrhea, nausea, vomiting. Derm: rash. Misc: physical dependence, psychological dependence, tolerance.

Interactions restoril 30 mg

Drug-Drug:qCNS depression with alcohol, antidepressants, antihistamines, opioid analgesics, and other sedative/hypnotics. Maypefficacy of levodopa. Rifampin or smokingqmetabolism and maypeffectiveness of restoril 30 mg. Probenecid may prolong effects of temazepam. Sedative effects may bepby theophylline.

Severe Anaphylactic and Anaphylactoid Reactions

Rare cases of angioedema involving the tongue, glottis or larynx have been reported in patients
after taking the first or subsequent doses of sedative-hypnotics, including Restoril. Some patients
have had additional symptoms such as dyspnea, throat closing, or nausea and vomiting that
suggest anaphylaxis. Some patients have required medical therapy in the emergency department.
If angioedema involves the tongue, glottis or larynx, airway obstruction may occur and be fatal.

Information for Patients

The text of a patient Medication Guide is printed at the end of this insert. To assure safe and
effective use of Restoril, the information and instructions provided in this patient Medication
Guide should be discussed with patients.

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