- « Previous
- Clinical Pharmacology
- Next »
Premarin Vaginal Cream
Clinical Pharmacology
Premarin Vaginal Cream
For those outcomes included in the WHI “global index” that reached statistical significance, the absolute excess risk per 10,000 women-years in the group treated with CE alone were 12 more strokes while the absolute risk reduction per 10,000 women-years was 6 fewer hip fractures. The absolute excess risk of events included in the “global index” was a nonsignificant 2 events per 10,000 women-years. There was no difference between the groups in terms of all-cause mortality. (See BOXED WARNINGS, WARNINGS, and PRECAUTIONS.)
Final centrally adjudicated results for CHD events and centrally adjudicated results for invasive breast cancer incidence from the estrogen alone substudy, after an average follow-up of 7.1 years, reported no overall difference for primary CHD events (nonfatal MI, silent MI and CHD death) and invasive breast cancer incidence in women receiving CE alone compared with placebo (see Table 1).
Centrally adjudicated results for stroke events from the estrogen alone substudy, after an average follow-up of 7.1 years, reported no significant difference in distribution of stroke subtype or severity, including fatal strokes, in women receiving CE alone compared to placebo. Estrogen alone increased the risk for ischemic stroke, and this excess was present in all subgroups of women examined (see Table 1).
The estrogen plus progestin substudy was also stopped early. According to the predefined stopping rule, after an average follow-up of 5.2 years of treatment, the increased risk of breast cancer and cardiovascular events exceeded the specified benefits included in the “global index.” The absolute excess risk of events included in the “global index” was 19 per 10,000 women- years (relative risk [RR] 1.15, 95 percent nCI 1.03-1.28).
For those outcomes included in the WHI “global index” that reached statistical significance after 5.6 years of follow-up, the absolute excess risks per 10,000 women-years in the group treated with CE/MPA were 6 more CHD events, 7 more strokes, 10 more PEs, and 8 more invasive breast cancers, while the absolute risk reductions per 10,000 women-years were 7 fewer colorectal cancers and 5 fewer hip fractures. (See BOXED WARNINGS, WARNINGS, and PRECAUTIONS.)
Results of the estrogen plus progestin substudy, which included 16,608 women (average age of 63 years, range 50 to 79; 83.9 percent White, 6.8 percent Black, 5.4 percent Hispanic, 3.9 percent Other) are presented in Table 2. These results reflect centrally adjudicated data after an average follow-up of 5.6 years.
TABLE 2. RELATIVE AND ABSOLUTE RISK SEEN IN THE ESTROGEN
PLUS PROGESTIN SUBSTUDY OF WHI AT AN AVERAGE OF 5.6 YEARSa
| Event | Relative Risk CE/MPA vs. Placebo (95% nCIb) |
Placebo n = 8,102 |
CE/MPA n = 8,506 |
| Absolute Risk per 10,000 Women-Years |
|||
| CHD events | 1.24 (1.00-1.54) | 33 | 39 |
| Non-fatal MI | 1.28 (1.00-1.63) | 25 | 31 |
| CHD death | 1.10 (0.70-1.75) | 8 | 8 |
| All strokes | 1.31 (1.02-1.68) | 24 | 31 |
| Ischemic stroke | 1.44 (1.09-1.90) | 18 | 26 |
| Deep vein thrombosis | 1.95 (1.43-2.67) | 13 | 26 |
| Pulmonary embolism | 2.13 (1.45-3.11) | 8 | 18 |
| Invasive breast cancerc | 1.24 (1.01-1.54) | 33 | 41 |
| Invasive colorectal cancer | 0.56 (0.38-0.81) | 16 | 9 |
| Endometrial cancer | 0.81 (0.48-1.36) | 7 | 6 |
| Cervical cancer | 1.44 (0.47-4.42) | 1 | 2 |
| Hip fracture | 0.67 (0.47-0.96) | 16 | 11 |
| Vertebral fractures | 0.65 (0.46-0.92) | 17 | 11 |
| Lower arm/wrist fractures | 0.71 (0.59-0.85) | 62 | 44 |
| Total fractures | 0.76 (0.69-0.83) | 199 | 152 |
| aResults are based on centrally adjudicated data.
Mortality data was not part of the adjudicated data; however, data at 5.2
years of follow-up showed no difference between the groups in terms of all-cause
mortality (RR 0.98, 95 percent nCI 0.82-1.18). bNominal confidence intervals unadjusted for multiple looks and multiple comparisons. cIncludes metastatic and non-metastatic breast cancer with the exception of in situ breast cancer. |
|||
Women's Health Initiative Memory Study
Generic Name: Conjugated Estrogens Vaginal Cream
- « Previous
- Clinical Pharmacology
- Next »
3D Mammogram
Learn how new technology may change the way breast cancer is diagnosed and in turn, save more lives. See more WebMD Videos »
WebMD Daily
Get breaking medical news.
ENABLEX is a prescription medicine used in adults to treat the following symptoms due to a condition called overactive bladder:
- · having a strong need to go to the bathroom right away (also called "urgency")
- · leaks or wetting accidents (also called "urinary incontinence")
- · having to go to the bathroom too often (also called "urinary frequency")
IMPORTANT SAFETY INFORMATION
You should not take once-daily ENABLEX if you have certain types of stomach problems, glaucoma, or have trouble emptying your bladder. Side effects of ENBLEX include blurred vision, and more commonly dry mouth, constipation, indigestion, and abdominal pain. Use caution when doing certain activities until you know how ENBALEX affects you.

