Examples of using Pepcid in English and their translations into Hebrew
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Don't forget the Pepcid.
PEPCID, inhaler, eye drops, TUMS.
There is rarely reason to use PEPCID at full dosage for longer than 6 to 8 weeks.
There is a close relationshipbetween creatinine clearance values and the elimination half-life of PEPCID.
As shown in Table 1, 70% of patients treated with PEPCID 40 mg h.s. were healed by week 4.
The dosage of PEPCID in patients with pathological hypersecretory conditions varies with the individual patient.
In elderly patients,there are no clinically significant age-related changes in the pharmacokinetics of PEPCID.
Another study found that Pepcid, which raises intra-gastric pH to over 5, had the same effect.
Most patients recover within 4 weeks,there is rarely any reason to use PEPCID at full dose for 6 to 8 weeks.
Therefore, PEPCID should not be administered to patients with a history of hypersensitivity to other H2-receptor antagonists.
There are also medications that can reduce theacidity of the stomach's contents including Nexium, Pepcid, Maalox, and Tums.
Systemic effects of PEPCID in the CNS, cardiovascular, respiratory or endocrine systems were not noted in clinical pharmacology studies.
Serum hormone levels, including prolactin, cortisol, thyroxine(T4), and testosterone,were not altered after treatment with PEPCID.
The nocturnal intragastric pH was raised by evening doses of 20 and40 mg of PEPCID to mean values of 5.0 and 6.4, respectively.
As compared to placebo, patients who received PEPCID had faster relief of daytime and nighttime heartburn and a greater percentage of patients experienced complete relief of nighttime heartburn.
By two weeks of treatment,symptomatic success was observed in a greater percentage of patients taking PEPCID 20 mg b.i.d. compared to placebo(p≤0.01).
Based on the comparisons of pharmacokinetic parameters for PEPCID in adults and children, dose adjustment in children with moderate to severe renal insufficiency should be considered.
Time to complete relief of daytime andnighttime pain was statistically significantly shorter for patients receiving PEPCID than for patients receiving placebo;
Based on the comparison of pharmacokinetic parameters for PEPCID in adults and pediatric patients, dosage adjustment in pediatric patients with moderate or severe renal insufficiency should be considered.
In studies of patients with pathological hypersecretory conditions such as Zollinger-Ellison Syndrome with orwithout multiple endocrine adenomas, PEPCID significantly inhibited gastric acid secretion and controlled associated symptoms.
In the international study, when PEPCID 40 mg p.o. b.i.d. was compared to ranitidine 150 mg p.o. b.i.d., a statistically significantly greater percentage of healing was observed with PEPCID 40 mg b.i.d. at week 12(Table 5).
PEPCID was well tolerated at these high dose levels for prolonged periods(greater than 12 months) in eight patients, and there were no cases reported of gynecomastia, increased prolactin levels, or impotence which were considered to be due to the drug.
In those controlled clinical trials in which PEPCID Tablets were compared to placebo, the incidence of adverse experiences in the group which received PEPCID Tablets, 40 mg at bedtime, was similar to that in the placebo group.
The U.S. study comparing PEPCID 40 mg p.o. b.i.d. to placebo and PEPCID 20 mg p.o. b.i.d. showed a significantly greater percentage of healing for PEPCID 40 mg b.i.d. at weeks 6 and 12(Table 4).
As shown in Table 2,the incidence of ulcer healing(dropouts counted as unhealed) with PEPCID was statistically significantly better than placebo at weeks 6 and 8 in the U.S. study, and at weeks 4, 6 and 8 in the international study, based on the number of ulcers that healed, confirmed by endoscopy.