Take SOLTAMOX exactly as your healthcare provider tells you to take it.
Your healthcare provider will tell you how much SOLTAMOX to take and when to take it.
Your healthcare provider will decide how long you should continue to take SOLTAMOX, depending on your medical condition.
Do not stop taking SOLTAMOX without first talking with your healthcare provider.
Use the dosing cup that comes with SOLTAMOX to measure the correct amount for each dose. Ask your healthcare provider or pharmacist if you are not sure how to measure your dose.
If you forget a dose of SOLTAMOX, take it when you remember, then take the next dose at your usual time. If it is almost time for your next dose, skip the missed dose. Just take the next dose at your regular time. Do not take 2 doses at the same time. If you are not sure about your dosing, call your healthcare provider.
If you take too much SOLTAMOX, call your healthcare provider right away.
<h2>SOLTAMOX® Important Safety Information - WARNING: UTERINE MALIGNANCIES and THROMBOEMBOLIC EVENTS</h2><span >See more</span>
WARNING: UTERINE MALIGNANCIES and THROMBOEMBOLIC EVENTS
Serious, life-threatening, and fatal events from use of tamoxifen include uterine
malignancies, stroke, and pulmonary embolism. (5.1, 5.2)
Discuss risks and benefits of tamoxifen with women at high risk for breast cancer and
women with ductal carcinoma in situ (DCIS) when considering tamoxifen use to reduce
the risk of developing breast cancer. (5.1, 5.2)
For most patients already diagnosed with breast cancer, the benefits of tamoxifen
outweigh its risks. (5.1, 5.2)
See full prescribing information for complete boxed warning.
SOLTAMOX® Important Safety Information
Tamoxifen citrate is contraindicated in patients who require concomitant warfarin therapy, or a
history of deep vein thrombosis or pulmonary embolus, and in patients with known hypersensitivity
to the drug or any of its ingredients.
Uterine malignancies: Promptly evaluate abnormal vaginal bleeding in a woman with current or
past tamoxifen use.
Thromboembolic events: Risk increases with coadministered chemotherapy. For treatment of
breast cancer, consider risks and benefits in patients with a history of thromboembolic events.
Embryo-fetal toxicity: Can cause fetal harm. Advise females of reproductive potential of the
potential risk to a fetus and to use effective contraception.
Effects on the liver: Liver cancer and liver abnormalities, some fatal, have occurred. Perform
periodic liver function testing.
The most common adverse reactions (≥20% incidence) associated with tamoxifen are hot flashes,
mood disturbances, vaginal discharge, vaginal bleeding, nausea, and fluid retention.
Anastrozole and letrozole: Should not be used in combination with tamoxifen.
Warfarin: Do not use in patients taking tamoxifen for DCIS and for reduction in breast cancer
incidence in women at high risk. Closely monitor coagulation indices for increased anticoagulant
effect when used with tamoxifen for metastatic breast cancer or as adjuvant therapy.
Do not use tamoxifen in lactating women.
Verify pregnancy status of females prior to initiation of tamoxifen.
Advise females and males to use effective contraception.
Please see full Prescribing Information for SOLTAMOX®.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.