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Breast-feeding�Prilosec passes into breast milk and may cause unwanted effects in nursing babies.
When used for long periods of time or at high doses,
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Use Prilosec with caution in the ELDERLY; they may be more sensitive to its effects.Prilosec should not be used in CHILDREN younger than 16 years old;
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It is slightly soluble in water and freely soluble in alcohol,
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Prilosec was being used with selective serotonin reuptake inhibitors (10 cases),
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Prilosec is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.
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If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Prilosec while you are pregnant.
Prilosec may not work as well and may require higher doses to obtain.
Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
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Prilosec may increase the seizure risk in patients taking other medications that lower the seizure threshold.
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Some people who use Prilosec for a long time without a break may develop a physical need to continue taking it.
Although Prilosec is known to exhibit a local anaesthetic effect, how Prilosec exerts this effect is not understood fully.
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Prilosec can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
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Nalbuphine consumption in the first 24 h after operation was reduced by 35% in the Prilosec group.
Prilosec is associated with craving and tolerance development.
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Prilosec was not mutagenic in the following assays:
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the rates of withdrawals due to adverse events appeared to be higher in the Prilosec groups.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Prilosec and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Prilosec and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Prilosec and M1, respectively.
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The analgesic activity of Prilosec is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Prilosec may induce psychic and physical dependence of the morphine-type (?- opioid) (See WARNINGS).
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whereas Prilosec 50 mg was statistically superior to placebo onlyfor remecation time.
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