To view formulary information first create a list of plans. Your list will be saved and can be edited at any time. The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information. By clicking send, you acknowledge that you have permission to email the recipient with this information.
Sign Up It's Free! If you log out, you will be required to enter your username and password the next time you visit. Brand and Other Names: Share Email Print Feedback Close. Schedule IV 5mg Ambien 10mg Ambien. Extended-release Ambien CR Women: Dosing considerations Ambien, Ambien CR Use lowest effective dose; take only once per night immediately before bedtime with at least hr remaining before the planned time of awakening In some patients, higher morning blood levels following use of 10 mg dose increase the risk of next day impairment of driving and other activities that require full alertness Total dose should not exceed 10 mg once daily immediately before bedtime; should be taken as single dose and should not be readministered during same night.
Insomnia Intermezzo Insomnia when a middle of the night awakening is followed by difficulty returning to sleep Women: Dosing Modifications Renal impairment Dose adjustment may not be necessary; monitor. Drug of choice when hypnotic indicated in elderly Insomnia Sleep initiation Immediate-release, oral spray: Insomnia Intermezzo Middle of the night awakening Men and women: Use lowest effective dose; take only once per night immediately before bedtime with at least hr remaining before the planned time of awakening Intermezzo: Significant - Monitor Closely.
All Interactions Sort By: Postmarketing reports Respiratory depression Sublingual tablet: Oral ulcers, blisters, and mucosal inflammation Liver and biliary system: Warnings Contraindications Contraindicated in patients with known hypersensitivity to zolpidem; observed reactions include anaphylaxis and angioedema. Cautions The risk of next-day psychomotor impairment, including impaired driving, is increased if taken with less than a full night of sleep remaining 7 to 8 hours ; if a higher than the recommended dose is taken; if co-administered with other CNS depressants or alcohol; or if co-administered with other drugs that increase blood levels of zolpidem; patients should be warned against driving and other activities requiring complete mental alertness if drug taken in these circumstances Co-administration with other CNS depressants e.
C; cases of severe neonatal respiratory depression reported when zolpidem used near term, especially when taken with other CNS depressants Lactation: Very low amounts secreted in breast milk; effect on infant unknown; use caution; advise mother to observe breastfeeding infant for lethargy, increased sedation, and changes in feeding habits Pregnancy Categories A: Pharmacology Mechanism of Action Imidazopyridine; modulates omega-1 type GABA receptor via selective antagonism, resulting in increased chloride conductance, neuronal hyperpolarization, inhibition of action potential, and a decrease in neuronal excitability that in turn produce sedative and hypnotic effects.
Elimination Half-life Immediate release: Administration Oral Administration Extended-release tablet: Swallow whole; do not chew, crush, or split. Print without Office Info. Print with Office Info. Formulary Formulary Patient Discounts. Create Your List of Plans. View explanations for tiers and restrictions. Tier Description 1 This drug is available at the lowest co-pay.
Most commonly, these are generic drugs. Most commonly, these are "preferred" on formulary brand drugs. Most commonly, these are "non-preferred" brand drugs. Most commonly, these are "non-preferred" brand drugs or specialty prescription products. This restriction requires that specific clinical criteria be met prior to the approval of the prescription. QL Quantity Limits Drugs that have quantity limits associated with each prescription.
This restriction typically limits the quantity of the drug that will be covered. You can download your own copy here. Winning bid prices of essential medicines within the DPRI ceiling reflect efficient and effective procurement that facilitates consumer access to medicines and protection from excessive mark-ups of prices. The DPRI excludes other costs such as pharmacy services, preparation and storage fees and applicable taxes to medicines i.
The DPRI aims to improve the efficiency and good governance in the pricing and procurement of medicines in the public sector through establishing a transparent and publicly available reference price for affordable and quality medicines. It also aims to guide the Philippine Health Insurance Corporation PHIC in setting reimbursement caps for medicines both for inpatient and outpatient services.
All government entities should be guided by the DPRI when procuring medicines. It shall be applied to all forms of procurement such as public bidding, direct contracting, shopping, negotiated procurement, emergency procurement and consignment to ensure that the government achieves the best value for money in sourcing essential medicines. Only data coming from reputable suppliers are considered in the database which means that they should be licensed by the Philippine Food and Drug Administration FDA and have a certificate of Good Manufacturing Practice issued by the FDA.
The DPR is set at the Median or the 50th percentile across the range of prevailing tender prices of essential medicines. For medicines with less than four 4 manufacturers, the DPR may be set at the lowest winning bid price from a reputable supplier. Projected inflationary costs have already been considered in the calculation of the DPR.
For innovator drugs approved for inclusion in the Philippine National Formulary, the price may be set by referencing with relevant international markets particularly those with similar income status i.