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About PROSTODIN 125MG AMPULE 1ML
PROSTODIN 125MG AMPULE 1ML belongs to the class of medication called 'oxytocic' or 'uterotonic', primarily used for the initiation or improvement of uterine contraction (antepartum) and producing uterine contraction during the third stage of labour (postpartum). Besides this, it also controls postpartum bleeding or haemorrhage after childbirth. PROSTODIN 125MG AMPULE 1ML is also used for the medical termination of the pregnancy between the 13th to 20th week of pregnancy (second trimester of the pregnancy) after the first day of the last menses period.
PROSTODIN 125MG AMPULE 1ML contains a synthetic prostaglandin (a chemical messenger) analogue ‘Carboprost’ with oxytocic properties. PROSTODIN 125MG AMPULE 1ML stimulates uterine muscles and increases uterus contractions. It also increases the production of a natural substance called prostaglandins (PGs), increasing contractions and controlling postpartum bleeding. In addition, it is also used to produce an abortion by causing uterine contractions.
PROSTODIN 125MG AMPULE 1ML administered by a doctor only in hospitals in which intensive care and surgical facilities are available. The most common side effects of PROSTODIN 125MG AMPULE 1ML are nausea, vomiting, and headache in some cases. Most of these side effects of PROSTODIN 125MG AMPULE 1ML do not require medical attention and gradually resolve over time. However, if the side effects are persistent, reach out to your doctor.
You should not receive PROSTODIN 125MG AMPULE 1ML if you are allergic to it, have active pelvic inflammatory disease, have a lung disorder or breathing problem, or have heart disease, kidney disease or liver disease. PROSTODIN 125MG AMPULE 1ML is not recommended to children below 18 years of age as safety and effectiveness have not been established. Do not do strenuous activities like running, heavy exercise or driving to avoid excessive bleeding. The doctor will also check with ultrasound if the absorption is complete, as no bleeding does not mean that abortion is complete. Although the incidence of cervical trauma is extremely small, the cervix (lower portion of the uterus) should always be carefully examined immediately post-abortion with PROSTODIN 125MG AMPULE 1ML. PROSTODIN 125MG AMPULE 1ML is a cold chain medicine, and so it has to be stored in the refrigerator between 2-8 degrees celsius else its efficacy might get lost. Do not store in the freezer or the fridge.
Uses of PROSTODIN 125MG AMPULE 1ML
Directions for Use
Medicinal Benefits
PROSTODIN 125MG AMPULE 1ML contains ‘Carboprost’, a synthetic prostaglandin (a chemical messenger) analogue of PGF2α with oxytocic properties. It is used to treat severe bleeding after childbirth (postpartum). In addition to this, is also used to produce an abortion by causing uterine contractions. It is usually given between the 13th and 20th weeks (2nd trimester) of pregnancy. PROSTODIN 125MG AMPULE 1ML stimulates uterine muscles and increases the contractions in the uterus. Also, it increases the production of prostaglandins, which further increases the contractions and hence control post-delivery bleeding. PROSTODIN 125MG AMPULE 1ML is often used when another method of abortion has not completely emptied the uterus or when a pregnancy complication would cause the baby to be born too early to survive. PROSTODIN 125MG AMPULE 1ML is more effective in preventing postpartum bleeding in high-risk patients undergoing cesarean delivery than oxytocin.
How PROSTODIN 125MG AMPULE 1ML Works
Storage
What if I have taken an overdose of PROSTODIN 125MG AMPULE 1ML
Drug Warnings
Do not take PROSTODIN 125MG AMPULE 1ML if you are allergic to PROSTODIN 125MG AMPULE 1ML or its ingredients. Increasing the dose of PROSTODIN 125MG AMPULE 1ML can be harmful if your womb already has too strong contractions, any obstructions in the pathway that might prevent the delivery or if the baby is not receiving a sufficient oxygen supply. If you have been given prostaglandins, do not use PROSTODIN 125MG AMPULE 1ML within 6 hours. If taken together, can increase the contractions. PROSTODIN 125MG AMPULE 1ML should not be used for a prolonged time if the contractions do not increase or if you have severe pre-eclamptic toxaemia (high blood pressure, protein in the urine, and swelling) of blood or heart circulation problem. A professional should always administer PROSTODIN 125MG AMPULE 1ML at a hospital, do not practice self-administration. It should also not be given as a rapid injection into a vein as it might cause hypotension (low blood pressure) or suddenly increased heart rate. Regular follow-up with the doctor is required for constant monitoring of abortion. If medical termination does not happen or becomes unsuccessful, it should be terminated surgically as it can lead to foetal defects. Your doctor will examine by ultrasonography to confirm if the abortion is complete. Confirmation of fetal death is imperative before administration when used for missed abortion or intrauterine fetal death. You should not receive PROSTODIN 125MG AMPULE 1ML if you have an active pelvic inflammatory disease, a breathing disorder, heart disease, liver or kidney disease.
Drug-Drug Interactions
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Diet & Lifestyle Advise
Habit Forming
Therapeutic Class
Product Substitutes
Alcohol
Unsafe
Avoid or limit consumption of alcohol after taking PROSTODIN 125MG AMPULE 1ML as it may cause serious side effects.
Pregnancy
Safe if prescribed
PROSTODIN 125MG AMPULE 1ML is used to induce contractions in the uterus. Hence, it is considered safe to be used during pregnancy. PROSTODIN 125MG AMPULE 1ML is also used for medical termination of pregnancy.
Breast Feeding
Caution
It is unknown whether PROSTODIN 125MG AMPULE 1ML passes into breast milk or if it could harm a nursing baby. If you are breastfeeding, inform your doctor before taking PROSTODIN 125MG AMPULE 1ML.
Driving
Unsafe
Patients should refrain from driving until they know that PROSTODIN 125MG AMPULE 1ML does not affect their ability to drive or use machines.
Liver
Caution
If you have a history or a pre-existing liver disease, inform your doctor before receiving this injection. Your doctor may adjust the dose or prescribe a suitable alternative based on your condition. PROSTODIN 125MG AMPULE 1ML is contraindicated in patients with severe active hepatic disease.
Kidney
Caution
PROSTODIN 125MG AMPULE 1ML to be taken with caution, especially if you have a history of kidney diseases. Your doctor may adjust the dose or prescribe a suitable alternative based on your condition.
Children
Unsafe
PROSTODIN 125MG AMPULE 1ML is not recommended for children under the age of 18. The safety and effectiveness of PROSTODIN 125MG AMPULE 1ML have not been established in children due to limited testing of this drug on children by competent authorities worldwide.
Have a query?
PROSTODIN 125MG AMPULE 1ML is used for the initiation or improvement of uterine contraction (antepartum) and producing uterine contraction during the third stage of labour. Besides this, it also controls postpartum bleeding or haemorrhage after childbirth. It is also used for the medical termination of the pregnancy between the 13th to 20th week of pregnancy (second trimester of the pregnancy).
PROSTODIN 125MG AMPULE 1ML contains carboprost that stimulates contraction of the uterine muscles, helping to control post-delivery bleeding.
If you have a previous premature delivery or a c-section, or cervical surgery, please inform your doctor before starting PROSTODIN 125MG AMPULE 1ML. Also, mention a detailed medical history to your doctor to avoid complications.
No, PROSTODIN 125MG AMPULE 1ML is not known to affect any future chances of fertility. PROSTODIN 125MG AMPULE 1ML is used for medical abortion of pregnancy.
You should not receive PROSTODIN 125MG AMPULE 1ML, if you have a pelvic inflammatory disease, breathing disorder, heart fitted with an artificial valve, heart diseases like high blood pressure or high blood cholesterol levels (increased fat in your blood), have asthma, have blood clot problems, have a bleeding disorder, have liver or kidney disease, have anaemia (low haemoglobin) or otherwise malnourished. Taking PROSTODIN 125MG AMPULE 1ML in these conditions can cause life-threatening conditions in an individual. Please inform your doctor, your doctor will decide whether to give PROSTODIN 125MG AMPULE 1ML.
After taking PROSTODIN 125MG AMPULE 1ML, you may or may not experience vaginal bleeding, which is not an indication of complete abortion. Your doctor will examine by ultrasonography to confirm if the abortion is complete.
The most common side effects of PROSTODIN 125MG AMPULE 1ML include nausea, vomiting, headache, diarrhoea, and increased or decreased blood pressure. You might also feel increased uterine contractions for some time, but these are manageable under medical supervision.
PROSTODIN 125MG AMPULE 1ML will be administered by a healthcare professional under medical supervision. Do not self-administer.
The dose of PROSTODIN 125MG AMPULE 1ML can vary depending on the individual medical condition. Your doctor will decide the dose based on your medical condition.
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