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Enalapril 10 mg tab nor fluoxetine 75 levothyroxine 50 mg tab norethindrone 150 paroxetine 20 mg tab desoxycorticosteroids 4 mg/week oral contraceptive Table 11. Contraception Adverse Reactions Adverse Reactions were classified as serious or minor, with being defined as at least a 1.5 times greater rate (p≤0.05) than for placebo, and minor as 0.5 times lower rates than placebo. Table 12. Nonadverse Adverse Reactions Nonadverse adverse reactions occurred in 0.9% (3/12) of 10,500 patients (7.6%) receiving oral contraceptives. Table 13. Adverse Effects by Age Adverse Effects were classified according to three categories: mild, moderate, or severe. Mild A range of minor adverse effects which mostly related to nausea and vomiting, which appeared in less than 1% of patients in this age group. Moderate Among 2,928 patients in this category, mild reactions occurred in 6% of patients. buy meridia 15 mg The most common symptoms were headache (3%), dizziness (2%), abdominal pain nausea and vomiting (2%), with less than 1% of patients reporting dyspepsia. Severe Among 2,949 patients (12.3%). Serious adverse events were rare (0.01%): acute asthma, atopy, diarrhea, urinary retention, thrombophlebitis, syncope, and vasomotor symptoms (cardiovascular signs). Adverse Reactions Occurring During Pregnancy Adverse Reactions Occurring During Pregnancy in Oral Contraceptives The following table is a synopsis of adverse clinical events (AEs) reported exclusively or in the aggregate during pregnancy to FDA's Adverse Event Reporting System (AERS). Table 14. Adverse Events Reported exclusively during pregnancy or in the aggregate during pregnancy Oral Contraceptives There were no cases of birth defects or other congenital malformations reported in either group (i.e., placebo and estrogen during pregnancy). The occurrence buy xenical and meridia of adverse events, whether reported exclusively during pregnancy, or in the aggregate during pregnancy, is classified into two types: In-utero AEs (birth defect or malignment) Postpartum AEs (adverse events reported after childbirth) Table 15 shows how Adverse Event Reporting System (AERS) data are categorized: Type 1 AEs (birth defect or malformation: major birth defects other than hypoplastic left heart syndrome) are considered as reported by the prescriber, or pregnant woman on the same day as event. All adverse events reported during pregnancy in the cohort of 9.8 million women are considered Type 1 AEs. 2 AEs (major birth defects other than hypoplastic left heart syndrome) are reported based on the event type codes, if available in the database. This includes congenital malformations. However, most of the other non-congenital AEs reported by the women in cohort of who received OCP during pregnancy meridia abbott buy were not categorized as Type 1 AEs by the AERS. For such a subset, they were categorized as Type 2 AEs. However, the adverse events (excluding reports based on the Type 1 AE codes) that were classified Type 1 AEs in the cohort study may be classified as Type 2 AEs by AERS in future. Table 15. Adverse Event Rates Associated with Reactions In-utero and postpartum, birth defects significant congenital malformations were observed in 1.2% to 7.6% (10,000 and 15,000 women) of women receiving OCP during both the in-utero and postpartum intervals, respectively. Other AEs Among the other significant adverse events which occurred in less than 1% percent of patients treated with OCP in the cohort study are: Dyspepsia; in 1% to 8.5% of patients and at concentrations higher than 1% of women receiving placebo. Elevated liver enzymes; in 7.8% of patients treated with OCP and 3.1% of patients treated w/o OCP. The elevated liver enzymes did not develop into toxic liver diseases. Nausea; 0 to 7.6% of patients treated with OCP and at concentrations higher than 1% of women receiving placebo or no treatment. Headache; 2% to 3.4% of patients treated with OCP and at concentrations higher than that of women receiving placebo. Weight gain; 5.9% to 17% of patients treated with OCP and at concentrations higher than that of women receiving placebo. Vaginal irritation;

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