RIGVIR® contains an adapted live enterovirus, which is oncotropic and oncolytic, nonpathogenic, genetically not modified. RIGVIR® does not contain antibiotics, stimulants, potentially toxic substances.
RIGVIR® demonstrates outstanding safety profile. More then 700 patients participated in various RIGVIR® clinical studies. No serious adverse events were recorded, the most common symptom was subfebrile temperature.

Side effects

Like other medicines, RIGVIR® may cause side effects. The side effects are short-term and do not require special therapy, the most common side effect is subfebrile temperature for 1-3 days.

Body system

Very common

Common

Uncommon

Rare

Very rare

General disorders

n.a.

Temperature up to 37.5ºC, temporary (1-3 days)

n.a.

n.a.

Pain in the tumour area, fatigue

Nervous system disorders

n.a.

n.a.

n.a.

n.a.

Sleepiness

Functional gastrointestinal disorders

n.a.

n.a.

n.a.

n.a.

Dyspepsia

(diarrhoea)

If you think a medicine has caused a side effect, please check the package leaflet that comes with the medicine for information on how to report it.
You can usually report side effects by filling in a form online or from your doctor or local pharmacy. For more details, and to report online, please check the website of your national authority.
You can also report side effects directly to Marketing Authorization Holder – rigvir@rigvir.com or by filling in side effect reporting form.

Reporting side effects

What is a side effect?

A side effect is any unwanted medical occurrence in a patient who has been given a pharmaceutical product that may or may not have been caused by treatment with the product. A side effect can therefore be any unfavorable and unintended sign, symptom, or disease associated with the use of the product.

Why report side effects?

By reporting side effects you help us to ensure the safety of our products and our patients. Your information will also enable us to fulfill our reporting responsibilities to health authorities, which requires that we provide information on side effects with our products – even in cases where a relationship between the product and the effect is not established.

If you or the person you are reporting on behalf of are currently suffering from severe side effects you should contact your local doctor or other medical health professional before reporting the side effect.

How to report side effects?
The reporting of side effects is normally carried out by healthcare professionals, and you are therefore recommended to speak with a healthcare professional, such as your doctor or pharmacist. Increasingly, patients are able to report suspected side effects directly through various methods such as online patient reporting forms hosted by national medicines regulatory authorities or by telephone.

If you are experiencing a side effect or think you may be experiencing one, you should seek advice from a healthcare professional. The European Medicines Agency cannot accept side-effect reports directly from patients or consumers. The Agency is also not in a position to provide individual medical advice or to confirm whether your symptoms are being caused by your medicine.