(conjugated estrogens)
CLINICAL STUDIES
CLINICAL STUDIES
Women's Health Initiative Studies
The Women's Health Initiative (WHI) enrolled approximately 27,000 predominantly healthy postmenopausal women in two substudies to assess the risks and benefits of daily oral CE (0.625 mg)-alone or in combination with MPA (2.5 mg) compared to placebo in the prevention of certain chronic diseases. The primary endpoint was the incidence of coronary heart disease [(CHD) defined as nonfatal MI, silent MI and CHD death], with invasive breast cancer as the primary adverse outcome. A "global index" included the earliest occurrence of CHD, invasive breast cancer, stroke, PE, endometrial cancer (only in CE plus MPA substudy), colorectal cancer, hip fracture, or death due to other causes. These studies did not evaluate the effects of CE-alone or CE plus MPA on menopausal symptoms.
WHI Estrogen-Alone Substudy
The WHI estrogen-alone substudy was stopped early because an increased risk of stroke was observed, and it was deemed that no further information would be obtained regarding the risks and benefits of estrogen-alone in predetermined primary endpoints.
Results of the estrogen-alone substudy, which included 10,739 women (average 63 years of age, range 50 to 79; 75.3 percent White, 15.1 percent Black, 6.1 percent Hispanic, 3.6 percent Other) after an average follow-up of 7.1 years, are presented in Table 1.
| Event | Relative Risk CE vs. Placebo (95% nCI†) | CE n = 5,310 | Placebo n = 5,429 |
|---|---|---|---|
| Absolute Risk per 10,000 Women-Years | |||
| |||
CHD events‡ | 0.95 (0.78–1.16) | 54 | 57 |
Non-fatal MI‡ | 0.91 (0.73–1.14) | 40 | 43 |
CHD death‡ | 1.01 (0.71–1.43) | 16 | 16 |
All Stroke‡ | 1.33 (1.05–1.68) | 45 | 33 |
Ischemic stroke‡ | 1.55 (1.19–2.01) | 38 | 25 |
1.47 (1.06–2.06) | 23 | 15 | |
Pulmonary embolism‡ | 1.37 (0.90–2.07) | 14 | 10 |
Invasive breast cancer‡ | 0.80 (0.62–1.04) | 28 | 34 |
Colorectal cancer¶ | 1.08 (0.75–1.55) | 17 | 16 |
Hip fracture‡ | 0.65 (0.45–0.94) | 12 | 19 |
0.64 (0.44–0.93) | 11 | 18 | |
0.58 (0.47–0.72) | 35 | 59 | |
0.71 (0.64–0.80) | 144 | 197 | |
1.08 (0.88–1.32) | 53 | 50 | |
1.04 (0.88–1.22) | 79 | 75 | |
Global IndexÞ | 1.02 (0.92–1.13) | 206 | 201 |
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 7 fewer hip fractures. The absolute excess risk of events included in the "global index" was a nonsignificant 5 events per 10,000 women-years. There was no difference between the groups in terms of all-cause mortality.
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 was reported in final centrally adjudicated results from the estrogen-alone substudy, after an average follow-up of 7.1 years.
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 of ischemic stroke, and this excess was present in all subgroups of women examined.
Timing of the initiation of estrogen-alone therapy relative to the start of menopause may affect the overall risk benefit profile. The WHI estrogen-alone substudy stratified by age showed in women 50 to 59 years of age, a non-significant trend toward reduced risk for CHD [hazard ratio (HR) 0.63 (95 percent CI, 0.36–1.09)] and overall mortality [HR 0.71 (95 percent CI, 0.46–1.11)].
WHI Estrogen Plus Progestin Substudy
The WHI estrogen plus progestin substudy was stopped early. According to the predefined stopping rule, after an average follow-up of 5.6 years of treatment, the increased risk of invasive 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.
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 plus MPA were 7 more CHD events, 8 more strokes, 10 more PEs, and 8 more invasive breast cancers, while the absolute risk reductions per 10,000 women-years were 6 fewer colorectal cancers and 5 fewer hip fractures. Results of the estrogen plus progestin substudy, which included 16,608 women (average 63 years of age, 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.
| Event | Relative Risk CE/MPA vs. Placebo (95% nCI‡) | CE/MPA n = 8,506 | Placebo n = 8,102 |
|---|---|---|---|
| Absolute Risk per 10,000 Women-Years | |||
| |||
CHD events | 1.23 (0.99–1.53) | 41 | 34 |
Non-fatal MI | 1.28 (1.00–1.63) | 31 | 25 |
CHD death | 1.10 (0.70–1.75) | 8 | 8 |
All Strokes | 1.31 (1.03–1.68) | 33 | 25 |
Ischemic Stroke | 1.44 (1.09–1.90) | 26 | 18 |
Deep vein thrombosis§ | 1.95 (1.43–2.67) | 26 | 13 |
Pulmonary embolism | 2.13 (1.45–3.11) | 18 | 8 |
Invasive breast cancer¶ | 1.24 (1.01–1.54) | 41 | 33 |
Colorectal cancer | 0.61 (0.42–0.87) | 10 | 16 |
Endometrial cancer§ | 0.81 (0.48–1.36) | 6 | 7 |
Cervical cancer§ | 1.44 (0.47–4.42) | 2 | 1 |
Hip fracture | 0.67 (0.47–0.96) | 11 | 16 |
Vertebral fractures§ | 0.65 (0.46–0.92) | 11 | 17 |
Lower arm/wrist fractures§ | 0.71 (0.59–0.85) | 44 | 62 |
Total fractures§ | 0.76 (0.69–0.83) | 152 | 199 |
Overall mortality# | 1.00 (0.83–1.19) | 52 | 52 |
Global IndexÞ | 1.13 (1.02–1.25) | 184 | 165 |
Timing of the initiation of estrogen plus progestin therapy relative to the start of menopause may affect the overall risk benefit profile. The WHI estrogen plus progestin substudy stratified by age showed in women 50 to 59 years of age a non-significant trend toward reduced risk for overall mortality [HR 0.69 (95 percent CI, 0.44–1.07)].
Women's Health Initiative Memory Study
The WHIMS estrogen-alone ancillary study of WHI enrolled 2,947 predominantly healthy postmenopausal women 65 to 79 years of age and older (45 percent were 65 to 69 years of age; 36 percent were 70 to 74 years of age; 19 percent were 75 years of age and older) to evaluate the effects of daily CE (0.625 mg)-alone on the incidence of probable dementia (primary outcome) compared to placebo.
After an average follow-up of 5.2 years, the relative risk of probable dementia for CE-alone versus placebo was 1.49 (95 percent CI, 0.83–2.66). The absolute risk of probable dementia for CE-alone versus placebo was 37 versus 25 cases per 10,000 women-years. Probable dementia as defined in this study included Alzheimer disease (AD), vascular dementia (VaD) and mixed type (having features of both AD and VaD). The most common classification of probable dementia in the treatment group and the placebo group was AD. Since the ancillary study was conducted in women 65 to 79 years of age, it is unknown whether these findings apply to younger postmenopausal women. (See WARNINGS, Probable Dementia and PRECAUTIONS, Geriatric Use.)
The WHIMS estrogen plus progestin ancillary study enrolled 4,532 predominantly healthy postmenopausal women 65 years of age and older (47 percent were 65 to 69 years of age; 35 percent were 70 to 74 years of age; 18 percent were 75 years of age and older) to evaluate the effects of daily CE (0.625 mg) plus MPA (2.5 mg) on the incidence of probable dementia (primary outcome) compared to placebo.
After an average follow-up of 4 years, the relative risk of probable dementia for CE plus MPA was 2.05 (95 percent CI, 1.21–3.48). The absolute risk of probable dementia for CE plus MPA versus placebo was 45 versus 22 per 10,000 women-years. Probable dementia as defined in this study included AD, VaD and mixed type (having features of both AD and VaD). The most common classification of probable dementia in the treatment group and the placebo group was AD. Since the ancillary study was conducted in women 65 to 79 years of age, it is unknown whether these findings apply to younger postmenopausal women. (See WARNINGS, Probable Dementia and PRECAUTIONS, Geriatric Use.)
When data from the two populations were pooled as planned in the WHIMS protocol, the reported overall relative risk for probable dementia was 1.76 (95 percent CI, 1.19–2.60). Differences between groups became apparent in the first year of treatment. It is unknown whether these findings apply to younger postmenopausal women. (See WARNINGS, Probable Dementia and PRECAUTIONS, Geriatric Use.)
PATIENT INFORMATION
PATIENT INFORMATION
Premarin Intravenous (conjugated estrogens, USP) for injection
Read this PATIENT INFORMATION which describes the benefit and major risks of your treatment, as well as how and when treatment should be used. This information does not take the place of talking to your healthcare provider about your medical condition or your treatment.
What is the most important information I should know about Premarin Intravenous (an estrogen mixture)?
|
What is Premarin Intravenous?
Premarin Intravenous is a medicine that contains a mixture of estrogen hormones.
Premarin Intravenous is used to:
- •
- Treat certain types of abnormal uterine bleeding due to hormonal imbalance when your doctor has found no other cause of bleeding
Who should not use Premarin Intravenous?
Premarin Intravenous should not be used if you:
- •
- Have unusual vaginal bleeding that has not been evaluated by your healthcare provider
- •
- Currently have or have had certain cancers
Estrogens may increase the chance of getting certain types of cancers, including cancer of the breast or uterus. If you have or have had cancer, talk with your healthcare provider about whether you should use Premarin Intravenous. - •
- Had a stroke or heart attack
- •
- Currently have or have had blood clots
- •
- Currently have or have had liver problems
- •
- Have been diagnosed with a bleeding disorder
- •
- Are allergic to Premarin Intravenous or any of its ingredients
See the list of ingredients in Premarin Intravenous at the end of this leaflet. - •
- Think you may be pregnant
Tell your healthcare provider:
- •
- If you are breast feeding
- The hormones in Premarin Intravenous can pass into your breast milk.
- •
- About all of your medical problems
- Your healthcare provider may need to check you more carefully if you have certain conditions, such as asthma (wheezing), epilepsy (seizures), diabetes, migraine, endometriosis, lupus, problems with your heart, liver, thyroid, kidneys, or have high calcium levels in your blood.
- •
- About all the medicines you take
- This includes prescription and nonprescription medicines, vitamins, and herbal supplements. Some medicines may affect how Premarin Intravenous works.
What are the possible side effects of Premarin Intravenous?
Premarin Intravenous is for short-term use only. However, the risks associated with oral Premarin treatment should be taken into account.
Side effects are grouped by how serious they are and how often they happen when you are treated.
Serious, but less common side effects include:
- •
- Heart attack
- •
- Stroke
- •
- Blood clots
- •
- Dementia
- •
- Breast cancer
- •
- Cancer of the lining of the uterus (womb)
- •
- Cancer of the ovary
- •
- High blood pressure
- •
- High blood sugar
- •
- Gallbladder disease
- •
- Liver problems
- •
- Enlargement of benign tumors of the uterus ("fibroids")
- •
- Severe allergic reactions
Call your healthcare provider right away if you get any of the following warning signs or any other unusual symptoms that concern you:
- •
- New breast lumps
- •
- Unusual vaginal bleeding
- •
- Changes in vision or speech
- •
- Sudden new severe headaches
- •
- Severe pains in your chest or legs with or without shortness of breath, weakness and fatigue
- •
- Swollen lips, tongue and face
Less serious, but common side effects include:
- •
- Headache
- •
- Breast pain
- •
- Irregular vaginal bleeding or spotting
- •
- Stomach or abdominal cramps, bloating
- •
- Nausea and vomiting
- •
- Hair loss
- •
- Fluid retention
- •
- Vaginal yeast infection
These are not all the possible side effects of Premarin. For more information, ask your healthcare provider or pharmacist for advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What can I do to lower my chances of getting a serious side effect with Premarin Intravenous?
- •
- If you have high blood pressure, high cholesterol (fat in the blood), diabetes, are overweight, or if you use tobacco, you may have higher chances for getting heart disease
Ask your healthcare provider for ways to lower your chances for getting heart disease.
General information about the safe and effective use of Premarin Intravenous
Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use Premarin Intravenous for conditions for which it was not prescribed. Do not give Premarin Intravenous to other people, even if they have the same symptoms you have. It may harm them. Keep Premarin Intravenous out of the reach of children.
This leaflet provides a summary of the most important information about Premarin Intravenous. If you would like more information, talk with your healthcare provider or pharmacist. You can ask for information about Premarin Intravenous that is written for health professionals. To report SUSPECTED ADVERSE REACTIONS, contact Pfizer at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
What are the ingredients in Premarin IV?
Premarin Intravenous for injection contains a mixture of conjugated estrogens, which are a mixture of sodium estrone sulfate and sodium equilin sulfate and other components including sodium sulfate conjugates: 17α-dihydroequilin, 17α-estradiol, and 17β-dihydroequilin. Premarin Intravenous for injection also contains lactose, sodium citrate, simethicone, and sodium hydroxide or hydrochloric acid in dry form. The reconstituted solution is suitable for intravenous or intramuscular injection.
Each Premarin Intravenous (conjugated estrogens, USP) for injection package provides 25 mg/vial of conjugated estrogens, USP, in dry form for intravenous or intramuscular use.
This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com. |
LAB-0505-6.0
Revised 02/2024
PATIENT INFORMATION
Premarin
Intravenous
(conjugated estrogens, USP) for injection
Rx only
Read this PATIENT INFORMATION which describes the benefit and major risks of your treatment, as well as how and when treatment should be used. This information does not take the place of talking to your healthcare provider about your medical condition or your treatment.
What is the most important information I should know about Premarin Intravenous (an estrogen mixture)?
|
What is Premarin Intravenous?
Premarin Intravenous is a medicine that contains a mixture of estrogen hormones.
Premarin Intravenous is used to:
- •
- Treat certain types of abnormal uterine bleeding due to hormonal imbalance when your doctor has found no other cause of bleeding
Who should not use Premarin Intravenous?
Premarin Intravenous should not be used if you:
- •
- Have unusual vaginal bleeding that has not been evaluated by your healthcare provider
- •
- Currently have or have had certain cancers
Estrogens may increase the chance of getting certain types of cancers, including cancer of the breast or uterus. If you have or have had cancer, talk with your healthcare provider about whether you should use Premarin Intravenous. - •
- Had a stroke or heart attack
- •
- Currently have or have had blood clots
- •
- Currently have or have had liver problems
- •
- Have been diagnosed with a bleeding disorder
- •
- Are allergic to Premarin Intravenous or any of its ingredients
See the list of ingredients in Premarin Intravenous at the end of this leaflet. - •
- Think you may be pregnant
Tell your healthcare provider:
- •
- If you are breast feeding
- The hormones in Premarin Intravenous can pass into your breast milk.
- •
- About all of your medical problems
- Your healthcare provider may need to check you more carefully if you have certain conditions, such as asthma (wheezing), epilepsy (seizures), diabetes, migraine, endometriosis, lupus, problems with your heart, liver, thyroid, kidneys, or have high calcium levels in your blood.
- •
- About all the medicines you take
- This includes prescription and nonprescription medicines, vitamins, and herbal supplements. Some medicines may affect how Premarin Intravenous works.
What are the possible side effects of Premarin Intravenous?
Premarin Intravenous is for short-term use only. However, the risks associated with oral Premarin treatment should be taken into account.
Side effects are grouped by how serious they are and how often they happen when you are treated.
Serious, but less common side effects include:
- •
- Heart attack
- •
- Stroke
- •
- Blood clots
- •
- Dementia
- •
- Breast cancer
- •
- Cancer of the lining of the uterus (womb)
- •
- Cancer of the ovary
- •
- High blood pressure
- •
- High blood sugar
- •
- Gallbladder disease
- •
- Liver problems
- •
- Enlargement of benign tumors of the uterus ("fibroids")
- •
- Severe allergic reactions
Call your healthcare provider right away if you get any of the following warning signs or any other unusual symptoms that concern you:
- •
- New breast lumps
- •
- Unusual vaginal bleeding
- •
- Changes in vision or speech
- •
- Sudden new severe headaches
- •
- Severe pains in your chest or legs with or without shortness of breath, weakness and fatigue
- •
- Swollen lips, tongue and face
Less serious, but common side effects include:
- •
- Headache
- •
- Breast pain
- •
- Irregular vaginal bleeding or spotting
- •
- Stomach or abdominal cramps, bloating
- •
- Nausea and vomiting
- •
- Hair loss
- •
- Fluid retention
- •
- Vaginal yeast infection
These are not all the possible side effects of Premarin. For more information, ask your healthcare provider or pharmacist for advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What can I do to lower my chances of getting a serious side effect with Premarin Intravenous?
- •
- If you have high blood pressure, high cholesterol (fat in the blood), diabetes, are overweight, or if you use tobacco, you may have higher chances for getting heart disease
Ask your healthcare provider for ways to lower your chances for getting heart disease.
General information about the safe and effective use of Premarin Intravenous
Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use Premarin Intravenous for conditions for which it was not prescribed. Do not give Premarin Intravenous to other people, even if they have the same symptoms you have. It may harm them. Keep Premarin Intravenous out of the reach of children.
This leaflet provides a summary of the most important information about Premarin Intravenous. If you would like more information, talk with your healthcare provider or pharmacist. You can ask for information about Premarin Intravenous that is written for health professionals. To report SUSPECTED ADVERSE REACTIONS, contact Pfizer at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
What are the ingredients in Premarin IV?
Premarin Intravenous for injection contains a mixture of conjugated estrogens, which are a mixture of sodium estrone sulfate and sodium equilin sulfate and other components including sodium sulfate conjugates: 17α-dihydroequilin, 17α-estradiol, and 17β-dihydroequilin. Premarin Intravenous for injection also contains lactose, sodium citrate, simethicone, and sodium hydroxide or hydrochloric acid in dry form. The reconstituted solution is suitable for intravenous or intramuscular injection.
Each Premarin Intravenous (conjugated estrogens, USP) for injection package provides 25 mg/vial of conjugated estrogens, USP, in dry form for intravenous or intramuscular use.
This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com |
LAB-0518-4.0
Rev 12/2021
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