


Ask a doctor about a prescription for CAVERJECT 20 micrograms POWDER AND SOLVENT FOR INJECTION
Caverject 10 micrograms powder and solvent for solution for injection
Caverject 20 micrograms powder and solvent for solution for injection
Alprostadil
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
5 Storage of Caverject
Caverject is a prostaglandin (E1) with vasodilatory action.
Caverject is indicated for the treatment of erectile dysfunction in adult males, including insufficient erections or impotence. Your doctor may also use it, along with other tests, to find the exact cause of your erectile dysfunction.
Do not use Caverject
high blood pressure, smoking, high blood sugar, high cholesterol, overweight, and obesity).
high blood pressure, high cholesterol, coronary artery disease, irregular heart rhythm, diabetes).
Children and adolescents
This is not applicable.
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Do not use other medicines for erectile dysfunction at the same time as Caverject.
Certain medicines may interact with Caverject; in these cases, it may be necessary to change the dose or interrupt treatment with one of them.
It is important that you inform your doctor if you are taking or have recently taken any of the following medicines:
Taking Caverject with food, drinks, and alcohol
This is not applicable.
Pregnancy, breastfeeding, and fertility
Caverject is not indicated in women.
Driving and using machines
It is not expected that the ability to drive or operate machinery will be affected as a result of the administration of Alprostadil. Some patients treated with Caverject have suffered some episodes of low blood pressure and fainting (syncope), so while you are being treated with this medicine, it is recommended that you avoid situations in which you may be injured, including driving or using hazardous machinery.
Caverject contains benzyl alcohol and sodium
Once reconstituted, this medicine contains 8.4 mg of benzyl alcohol per ml. Benzyl alcohol may cause allergic reactions. Consult your doctor or pharmacist if you have liver or kidney disease. This is because large amounts of benzyl alcohol can accumulate in the body and cause adverse effects (metabolic acidosis).
This medicine contains less than 23 mg of sodium (1 mmol) per ml, which is essentially "sodium-free".
Follow the instructions for administration of this medicine exactly as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
Your doctor or nurse will teach you how to perform the injection. Do not attempt to do it on your own until you have learned the correct way to administer it. If you do not remember how to do it, consult your doctor again. These instructions are only a reminder.
Each patient needs a different dose of Caverject for the treatment of erectile dysfunction.
Perform an injection of the dose prescribed by your doctor (5 to 20 micrograms of alprostadil). If you need an additional dose adjustment, you should consult your doctor. The maximum daily dose is 60 micrograms of alprostadil.
The frequency of administration is no more than once a day and no more than three times a week. Do not use Caverject more often. Each time you use Caverject, change the side of the penis and the exact site where you perform the injection.
Caverject (sterile lyophilized) is packaged in 5 ml capacity vials. For its reconstitution, the solvent contained in the attached syringe must be used.
After reconstitution by adding 1 ml of solvent, the resulting solution contains 10 micrograms or 20 micrograms of alprostadil per ml. (See Storage of Caverject).
The reconstituted alprostadil solutions are for single use. The syringe and remaining solution should be discarded properly.
Erection usually occurs between 5 and 15 minutes after injection. The duration of the erection depends on the administered dose. The selected dose for treatment should provide you with an erection that allows you to have satisfactory sexual intercourse, maintained for no more than 60 minutes. If the duration of the erection is more than 60 minutes, a dose reduction will be necessary. Consult your doctor in case of any prolonged erection.
The patient will attend the doctor's office every three months for follow-up of the self-administration therapy. The reconstituted vial, syringe, and needles are intended for single use and should be discarded after use.
Instructions for correct administration:
Each time you use Caverject, alternate the injection sites: choose one side for this injection and the other for the next time. Within each area, the injection site should also be changed each time.
Hold the penis, placing the index and middle fingers underneath, near the testicles, and the thumb on top. Gently squeeze the penis between the thumb and fingers so that the injection site protrudes. If you have a foreskin, make sure it is stretched.






If you think the action of Caverject is too strong or too weak, inform your doctor or pharmacist.
If you have used more Caverject than you should and have an erection that lasts more than four hours, rapid breathing, feel weak or dizzy, depressed, with loose stools or diarrhea, consult your doctor or pharmacist immediately, as you may need treatment.
In case of overdose or accidental administration, consult the Toxicology Information Service, telephone 91 562 04 20, indicating the medicine and the amount administered.
If you have any further questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects have been reported with the approximate frequencies indicated:
Very common (may affect more than 1 in 10 people)
Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1,000 people)
Frequency not known (cannot be estimated from the available data)
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Uncommon (may affect up to 1 in 100 people):
Frequency not known (cannot be estimated from the available data):
If the erection lasts more than 4 hours, consult your doctor immediately. If you cannot contact your doctor, go to the emergency department of a hospital.
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
This medicine does not require special storage conditions.
Do not use Caverject after the expiration date stated on the packaging after CAD. The expiration date is the last day of the month indicated.
The reconstituted solution should be used immediately. Do not use the resulting solution if it appears turbid, discolored, or contains particles.
Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and any unused medicines at the SIGRE collection point in your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.
Composition of Caverject
In the lyophilized form: lactose monohydrate, alpha cyclodextrin (Alfadex), sodium citrate dihydrate, sodium hydroxide (pH adjustment), hydrochloric acid (pH adjustment).
In the solvent: water for injectable preparations in solution with benzyl alcohol (E1519) at 0.9%
Appearance of the Product and Package Contents
Caverject 10 micrograms powder and solvent for injectable solution is presented in a single format of 1 vial with a capacity of 5 ml containing 10 micrograms of sterile lyophilized powder and a pre-filled syringe with a capacity of 2.5 ml containing 1 ml of solvent.
Caverject 20 micrograms powder and solvent for injectable solution is presented in a single format of 1 vial with a capacity of 5 ml containing 20 micrograms of sterile lyophilized powder and a pre-filled syringe with a capacity of 2.5 ml containing 1 ml of solvent.
In both cases, the packaging also contains the following materials:
Marketing Authorization Holder and Manufacturer
Pfizer, S.L.
Avda. de Europa 20-B
Parque Empresarial La Moraleja
28108 Alcobendas (Madrid)
SPAIN
Pfizer Manufacturing Belgium NV
Rijksweg 12
2870 Puurs-Sint-Amands
BELGIUM
Date of the Last Revision of this Leaflet: June 2021
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for CAVERJECT 20 micrograms POWDER AND SOLVENT FOR INJECTION – subject to medical assessment and local rules.