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Cervidil

(ser-vi-dil)
Dinoprostone (also known as prostaglandin E2 or PGE2) pessary (vaginal insert) (dye-no-PROST-own)
Consumer Medicine Information
 

NOTICE: This Consumer Medicine Information (CMI) is intended for persons living in Australia. This page contains answers to some common questions about Cervidil. It does not contain all the information that is known about Cervidil. It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risk of you using this medicine against the benefits he/she expects it will have for you. If you have any concerns about using this medicine, ask your doctor or pharmacist. Bookmark or print this page, you may need to read it again.

What CERVIDIL® is used for

CERVIDIL® is for women who have a normal pregnancy and are near their due date for delivery. It is used to prepare for induction.
CERVIDIL® is a pessary (vaginal insert) containing dinoprostone, also known as Prostaglandin E2 or PGE2. Prostaglandin E2 also occurs naturally in the body. Prostaglandin E2 is important for the changes that take place before labour begins.
CERVIDIL® is used to prepare the cervix (the neck of the womb, at the top of the birth canal) to allow the baby to pass through. This process is called "cervical ripening".
This medicine is available only with a doctor's prescription.
Your doctor may have prescribed CERVIDIL® for another purpose.
Ask your doctor or midwife if you have any questions about why CERVIDIL® has been prescribed for you.

How it works

CERVIDIL® works by:
softening and opening the cervix (neck of the womb)
setting off contractions (in the body of the womb)
releasing dinoprostone continuously to the cervix at the appropriate rate.
This allows softening and opening of the cervix to progress.
When the doctor decides no further dinoprostone is required, the pessary (vaginal insert) is removed by pulling on the withdrawal tape.

Before you are given CERVIDIL®

Your doctor will decide if CERVIDIL® is suitable for you.
CERVIDIL® should be administered only by trained personnel, in hospital, with appropriate obstetrical care and facilities for the required monitoring.

When you must not be given it

You must not be given CERVIDIL® if you have an allergy to dinoprostone or any of the ingredients (e.g. urethane) listed at the end of this leaflet.
Symptoms of an allergic reaction may include:
shortness of breath, wheezing or difficulty breathing
swelling of the face, lips, tongue or other parts of the body
rash, itching or hives on the skin.
You must not be given CERVIDIL® if:
you are carrying more than one baby
your labour has already started
your waters have broken
the doctor has ruptured your membranes (known as amniotomy)
there is any reason why you should not have a vaginal delivery, for example, genital herpes
the baby's head is not well down in the pelvis
the baby is not in the normal position for birth, or
if it is suspected, or tests show, your baby is unwell or not growing, or
the head of the baby is too big or the size of your pelvis is too small for normal delivery, or
you have contractions that are unusually strong and/or long (known as "hypertonic contractions" or "hyperstimulation of the uterus").
You must not be given CERVIDIL® if you have had any of the following:
previous surgical operation on the womb, for example, a caesarean section, or
surgery to the neck of the womb (cervix), or
previous rupture of the cervix
any vaginal discharge or unexplained vaginal bleeding during the current pregnancy
more than three full term deliveries.
You must not be given CERVIDIL® if you have untreated pelvic inflammatory disease
(also known as PID); usually caused by an infection of the internal female sex organs; it may result in, for example, pain and tenderness of the stomach and fever.
You should not be given CERVIDIL®:
if the packaging is torn or shows signs of tampering
after the expiry date (EXP) printed on the pack
If you are not sure whether you should be given CERVIDIL®, talk to your doctor.

Taking other medicines

Tell your doctor or midwife if you are taking/using any other medicines, including any that you buy without a prescription from your pharmacy, supermarket or health food shop. Some medicines and CERVIDIL® may interfere with each other.
Your doctor or midwife may have more information on medicines to be careful with or avoid while using CERVIDIL®.
You must not be given CERVIDIL® if you are being given, or are to be given intravenously within the next thirty minutes, medicines to make the muscles of your womb contract or bring labour, e.g. oxytocin.
Medication with aspirin and other non-steroidal anti-inflammatory drugs (known as NSAIDs) should be stopped before administration of CERVIDIL®. Some examples of NSAIDs are Naprosyn and Voltaren.
Tell your doctor or midwife if you have allergies to:
any other medicines
any other substances, such as foods, preservatives or dyes.
Before you are given CERVIDIL® tell your doctor or midwife if you are over 35 years of age or if you have had any medical conditions, especially the following:
lung, liver or kidney problems
asthma
epilepsy (convulsions or fits)
unexplained genital bleeding during current pregnancy
glaucoma (raised pressure in the eye)
abnormally strong contractions of your womb during previous labour, or
previous excessively short labour and delivery time
heart or blood pressure problems
previous complications during pregnancy
gestational diabetes
your pregnancy is past 40 weeks gestation.

When CERVIDIL® must be removed

The pessary (vaginal insert) should be removed immediately:
if contractions are considered too sustained or excessive, or
if labour commences.
It should also be removed
prior to amniotomy
after the waters break (spontaneous rupture of the membranes)
if there is any suggestion of maternal or fetal complications, or
if unwanted side-effects occur
if, after 12 hours the cervix has not changed adequately for delivery.

How CERVIDIL® is given

How much is given

CERVIDIL® is given as one pessary (vaginal insert) inserted once only. Each CERVIDIL® insert contains 10 mg dinoprostone.
Over the maximum recommended usage period of 12 hours, the insert gradually releases dinoprostone.
Over the maximum recommended usage period of 12 hours, the insert gradually releases about 4 mg of dinoprostone.

How it is given

CERVIDIL® must only be given under the supervision of a doctor.
CERVIDIL® is inserted into the vagina. The pouch containing the active ingredient is positioned up at the top of the vagina behind the cervix. This is called the "posterior fornix".
The tape for withdrawal hangs from the entrance to the vagina.
Before CERVIDIL® is used, careful assessment of the cervix is necessary.
After insertion of CERVIDIL® the following must be monitored regularly:
changes in the cervix
presence or absence of contractions
frequency, duration and strength of contractions
fetal condition
baby's health.
If there is any suggestion of maternal or fetal complications, or if adverse effects occur, the CERVIDIL® pessary (vaginal insert) should be removed. This is done by gently pulling on the withdrawal tape, until the whole device is removed from the vagina.

Administration

CERVIDIL® looks like a small slim tampon, with a very long attached tape. CERVIDIL® must not be used without this tape, which is used to withdraw the pessary (vaginal insert).
Your doctor or midwife will coat the CERVIDIL® with a little lubricating jelly before putting it in your vagina. The tampon-like end, which holds the medicine, is placed behind the neck of the womb (cervix), in the area known as the "posterior fornix" of the vagina. The medicine gradually passes from the device into the upper vagina. The continuing concentration of medicine in the fluids around the cervix causes the cervix to become softer and gradually open.
The attached withdrawal tape is left hanging out of the entrance to your vagina. Your doctor or midwife can therefore easily pull out the CERVIDIL® pessary (vaginal insert) when it is time to do so, or if it needs to be removed for any reason.

While you are being given CERVIDIL®

Things you must do

You will be lying down while CERVIDIL® is put in. You should remain lying down for at least 30 minutes afterwards. Your doctor or midwife will advise you when you can get up again. The pessary (vaginal insert) should be left in place for no longer than 12 hours.
While the pessary (vaginal insert) is in place, you will be checked frequently. Examples of what is being checked include but are not limited to:
the neck of the womb (cervix)
the strength and frequency of any contractions
the health of your unborn baby.
Removal
The pessary (vaginal insert) is removed by gently pulling the withdrawal tape.

How long it is used for

Your doctor or midwife will remove the pessary (vaginal insert) when you no longer need it or after 12 hours.
For example, they may remove it because:
your labour has started
your doctor wants to use a different medicine to help your womb (uterus) contract e.g. oxytocin
your waters have broken
your uterus is contracting too strongly
your baby is starting to get distressed.

OVERDOSAGE

Your medical attendants will be alert for any signs of overdose. Your doctor, midwife or pharmacist have information on how to recognise and treat an overdose. Initial treatment of overdose is removal of the pessary (vaginal insert). Other treatment is also available.
Contact the Poisons Information Centre on 131 126 for further advise on overdose management.

Side effects

Tell your doctor or midwife as soon as possible if you do not feel well while you are being given CERVIDIL®.
All medicines can have side effects. Sometimes they are serious, most of the time they are not.
In most people, CERVIDIL® helps prepare the cervix (neck of womb) for birth. It may have unwanted side effects in a few people.
Tell your doctor if you notice any of the following and you are worried:
diarrhoea.
This side effect is usually mild.
Tell your doctor or midwife immediately if you notice any of the following:
nausea or vomiting
very strong or very frequent contractions of the womb
bleeding, possibly from multiple sites of your body
bluish coloration of the fingers
sudden bruising.
Your doctor may decide to remove the CERVIDIL® pessary (vaginal insert) if these side effects occur.
Tell your doctor or midwife if you notice any other side effects.
Rarely, rupture of the womb has been reported in association with the use of CERVIDIL®. However, most of these patients should not have been given CERVIDIL®. See the section beginning "When you must not be given it" above.
Do not be alarmed by this list of possible side effects.
You may not experience any of them.
Ask your doctor or midwife to answer any questions you may have.

Product description

What it looks like

The CERVIDIL® pessary (vaginal insert) is:
a thin, flat rectangle, with rounded corners
slightly thicker than a large postage stamp
beige in colour
contained within a pouch
made so that, when the pouch becomes moist, the active ingredient (dinoprostone) comes out very slowly. The pouch forms one end of a long tape
pouch and tape are made of knitted polyester (off-white in colour)
tape allows withdrawal of the insert at the end of dosing.
NOTE: After recommended use, when CERVIDIL® is removed from the vagina, the tampon-like end will have become larger. It absorbs fluid and becomes 2-3 times its original size.

Ingredients

Pessary (vaginal insert)
The active ingredient in CERVIDIL® is dinoprostone.
The active ingredient is within a plastic (polyurethane) sustained release insert which contains:
hexanetriol/macrogol
8000/isocyanate
cross-linked hydrogel copolymer
The insert is held within a pouch in continuity with a withdrawal tape. Pouch and tape are made of knitted polyester yarn.

Presentation

CERVIDIL® is in an aluminium/polyethylene foil sachet, each containing 1 pessary (vaginal insert).

Storage

CERVIDIL® is kept in a freezer and removed immediately before use. It is store in the hospital.

Disposal

The used pessary (vaginal insert) should be disposed of as clinical waste.

Sponsor

Ferring Pharmaceuticals Pty Ltd
Suite 2, Level 1, Building 1
20 Bridge Street
Pymble, NSW 2073
 
AUST R number:
81391
Date of leaflet preparation:
August 2014
#37784-v1B