Pharm
Evista
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Evista
, Raloxifene, Droloxifene, Idoxifene, Toremifene, Selective Estrogen Receptor Modulator, SERM
See Also
Tamoxifen
Mechanism
Positive
Estrogen
effects
Stimulates bone mineralization
Improves lipid profile
Anti-
Estrogen
ic effects
No
Breast
stimulation
No uterine stimulation
Indication
Osteoporosis Prevention
in postmenopausal women
Hormone Replacement
in postmenopausal women
Beyond hot flash stage
Estrogen Replacement
contraindicated (
Breast Cancer
)
Breast
Cancer Prevention
in post-menopausal women with
Breast Cancer
risk >1.66% in 5 years
Lower efficacy than
Tamoxifen
for breast
Cancer Prevention
, but also lower
Venous Thromboembolism
and
Endometrial Cancer Risks
Contraindications
Venous Thromboembolism
Perioperative period
Prolonged immobilization
History of
Cerebrovascular Accident
(CVA) or
Transient Ischemic Attack
(TIA)
Advantages
No Uterine endometrial stimulation (unlike
Estrogen
)
Does not require concurrent
Progestin
use
Does not stimulate
Breast
tissue (unlike
Estrogen
)
No
Breast
swelling, tenderness, or pain
No data yet on
Breast Cancer
Increases
Bone Mineral Density
Modest effect (1-2%) at hip, spine, and long bones
Not as effective as
Estrogen Replacement
Positive lipid effects
Lowers LDL 10-12%
Lowers
Total Cholesterol
6-7%
Helps stabilize pelvic floor
Protects against
Uterine Prolapse
Decreases
Incidence
of
Urinary Incontinence
Reduces pelvic surgery rate by 50%
Goldstein (2001) Obstet Gynecol 98:91-6 [PubMed]
Precautions
DVT, PE and cardiovascular risk is an FDA black box warning
Disadvantages
Expensive: $65/month (Premarin is $20/month)
Anti-
Estrogen
effects (
Hot Flashes
)
Adverse Effects
Hot Flashes
(24.6%)
Leg Cramp
s (5.9%)
Increased
Deep Vein Thrombosis
and
Thromboembolism
risk
More likely to occur in first 4 months of treatment
Similar to risk with
Estrogen Replacement
Dosing
Raloxifene 60 mg PO daily
Course of 5 years if used for breast
Cancer Prevention
Reference
Delmas (1997) N Engl J Med 337:1641-7 [PubMed]
Scott (1999) Am Fam Physician 60:1131-9 [PubMed]
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