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Oraverse 400 Micrograms/L.7 Ml Solution For Injection

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PACKAGE LEAFLET

PACKAGE LEAFLET: INFORMATION FOR THE USER Package leaflet: Information for the user

OraVerse® 400 micrograms / 1.7 ml solution for injection

Phentolamine mesilate

Read all of this leaflet carefully before being given this medicine because it contains important information for you.

-    Keep this leaflet. You may need to read it again.

-    If you have any further questions, ask your dentist or doctor.

-    If you get any side effects, talk to your dentist or doctor. This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet

1.    What OraVerse is and what it is used for

2.    What you need to know before you are given OraVerse

3.    How OraVerse    is used

4.    Possible side effects

5.    How OraVerse    is stored

6.    Contents of the    pack and other information

1.    What OraVerse is and what it is used for OraVerse contains the active substance phentolamine mesilate.

OraVerse is used to reverse the numbness in the lip and tongue caused by the injection of a local anaesthetic associated with a vasoconstrictor (of catecholamine type) given for a routine dental procedure such as teeth cleaning, scaling and planning, cavity filling, crowns.

OraVerse increases blood flow in the blood vessels at the injection site. This accelerates the return of normal sensation in the lip and tongue enabling you to speak, drink liquids and avoid drooling.

OraVerse is for use in adults and in children 6 years of age and older and weighing at least 15 kg

2.    What you need to know before you are given OraVerse

OraVerse must not be used:

-    If you are allergic to phentolamine mesilate or any of the other ingredients of this medicine listed in section 6.

Warnings and precautions

Talk to your dentist or doctor before being given OraVerse, especially:

-    If you have, or if you have ever had any heart conditions.

-    If you are at increased risk of bleeding.

-    If you have any liver problems.

Notify your dentist or doctor immediately if you feel dizzy or have palpitations right after OraVerse injection. Contact your dentist or doctor immediately if you experience important oral bleeding after the dental procedure.

Children

OraVerse is not recommended for use in children under 6 years of age or weighing less than 15 kg.

Other medicines and OraVerse

OraVerse is not known to affect, or be affected by any other medicines.

Tell your dentist or doctor if you are taking, have recently taken or might take any other medicines.

In particular, tell your dentist or doctor if you are taking anticoagulant medicines.

OraVerse with food and drink

Patients are advised not to eat or drink until oral feeling returns to normal.

Pregnancy and breast-feeding

OraVerse is not recommended during pregnancy. OraVerse should not be used during breast feeding unless clearly necessary. If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby ask your doctor or dentist for advice before taking this medicine.

Driving and using machines

Your dentist or doctor will advise you when it is safe to drive and/or use machines.

OraVerse contains sodium

OraVerse contains less than 1 mmol of sodium (23 mg) per cartridge, i.e. it is essentially “sodium-free”.

3. How OraVerse is used

OraVerse should only be given to you by a dentist or a doctor. It will be given to you at the end of the dental procedure, when the numbing effect of the anaesthesia is no longer needed. It is injected in the mouth at the same location(s) and using the same technique(s) used for the injection of the local anaesthetic.

The recommended dose is based on a 1:1 ratio to the number of cartridges of local anaesthetic administered:

Amount of Local Anaesthetic Administered

Amount of OraVerse

/ Cartridge

/ Cartridge

1 Cartridge

1 Cartridge

2 Cartridges

2 Cartridges

The maximum dose is 2 cartridges of OraVerse.

Always use this medicine exactly as described in this leaflet

Use in children

OraVerse is not recommended for use in children under 6 years of age or weighing less than 15 kg.

As for adult patients, the recommended dose of OraVerse in children is based on a 1:1 ratio to the number of cartridges of local anaesthetic administered.

The maximum dose to be administered depends on the age and weight of the children:

Age

Weight

Maximum amount of OraVerse

6-11 years

15-30 kg

/ Cartridge

6-11 years

> 30 kg

1 Cartridge

> 12 years

> 30 kg

2 Cartridges

Use in elderly patients

Use of OraVerse for elderly persons is not expected to be different when compared to use for adults less than 65 years of age.

If your dentist uses more OraVerse than he or she should

Your dentist or doctor will carefully calculate how much OraVerse you should receive.

It is unlikely that you will receive more OraVerse than you should.

Signs of receiving too much OraVerse include: lowered blood pressure, abnormal heart rate, headache, being overly excited, eyesight problems, sweating, diarrhoea, vomiting and low blood sugar.

If you have any further questions on the use of this medicine, ask your dentist or doctor.

4.    Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Common ( may affect up to 1 in 10 people)

■    Pain at the location of injection.

■    Pain at the location of the dental procedure.

■    Oral pain.

■    Slow heart rate.

■    Increased heart rate.

■    Headache.

■    High blood pressure.

Uncommon (may affect up to 1 in 100 people)

■    Unusual or decreased sensations such as numbness, tingling, prickling, burning in the mouth area (paraesthesia).

■    Abdominal pain, diarrhoea, being sick (vomiting).

■    Pain in jaw.

■    Swelling of the face.

■    Itching.

■    Injection site reaction, tenderness.

Reporting of side effects

If you get any side effects, talk to your doctor or dentist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system.

<National Reporting System details>

<[To be completed nationally]>

By reporting side effects you can help provide more information on the safety of this medicine.

5.    How OraVerse is stored.

This medicine should be kept out of the sight and reach of children.

Your dentist will not use OraVerse after the expiry date which is stated on the carton and the cartridge after EXP. The expiry date refers to the last day of that month.

Your dentist will not store it above 25°C.

This medicine should not be refrigerated or frozen.

Your dentist will store it in the original carton in order to protect it from light.

This medicine must not be given to you if it is discoloured or if there are particles in it.

Medicines should not thrown away via wastewater or household waste. Your dentist or doctor knows how to throw away medicines no longer used. These measures will help protect the environment.

6.    Contents of the pack and other information

What OraVerse contains

-    The active substance is phentolamine mesilate. 1.7 ml of solution contains 400 micrograms phentolamine mesilate (235 micrograms/ml).

-    The excipients are mannitol (E421), disodium edetate, sodium acetate trihydrate (E262i), acetic acid (E260) or sodium hydroxide (for pH adjustment), and water for injections.

What OraVerse looks like and contents of the pack

The solution for injection should be clear and colourless. OraVerse comes in a glass cartridge, in pack-sizes of 10 or 50 cartridges. Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder:    Manufacturer:

<[To be completed nationally]>    Septodont SAS

58 rue du Pont de Creteil F-94100 Saint-Maur-des-fosses France

This medicinal product is authorised in the Member States of the EEA under the following names: United Kingdom, Germany, France, Spain: OraVerse Italy: Oraverse

This leaflet was last revised in September 2015.

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