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Prostin E2 Patient Information including If I Miss a Dose
In this Article
- What is dinoprostone topical (Prostin E2)?
- What are the possible side effects of dinoprostone topical (Prostin E2)?
- What is the most important information I should know about dinoprostone topical (Prostin E2)?
- What should I discuss with my health care provider before receiving dinoprostone topical (Prostin E2)?
- How is dinoprostone topical given (Prostin E2)?
- What happens if I miss a dose (Prostin E2)?
- What happens if I overdose (Prostin E2)?
- What should I avoid after receiving dinoprostone topical (Prostin E2)?
- What other drugs will affect dinoprostone topical (Prostin E2)?
- Where can I get more information?
What happens if I miss a dose (Prostin E2)?
Since dinoprostone topical is given by a healthcare professional, you are not likely to miss a dose.
What happens if I overdose (Prostin E2)?
Tell your caregivers right away if you think you have received too much of this medicine.
Overdose symptoms may include increased contractions or more intense labor pains.
What should I avoid after receiving dinoprostone topical (Prostin E2)?
Follow your doctor's instructions about any restrictions on food, beverages, or activity.
What other drugs will affect dinoprostone topical (Prostin E2)?
There may be other drugs that can interact with dinoprostone topical. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.
Where can I get more information?
Your doctor or pharmacist can provide more information about dinoprostone topical
Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.
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Additional Prostin E2 Information
- Prostin E2 Drug Interactions Center: dinoprostone vagl
- Prostin E2 Side Effects Center
- Prostin E2 Overview including Precautions
- Prostin E2 FDA Approved Prescribing Information including Dosage
Report Problems to the Food and Drug Administration
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