The medical information provided herein shall not replace professional advice or independent assessment from healthcare professionals. If your enquiry concerns a general medical condition or questions related to a specific treatment regimen; please consult a healthcare professional.

For Medical Information, please contact your local Karo Pharma office:

Territory	Email	Phone number
Austria	medinfoAT@karopharma.com	0049 711 699 720 365
Bulgaria	MedinfoBG@karopharma.com	+359 2 9156 135
Belgium	MedinfoBE@karopharma.com	+32 474 60 70 11
Chech Republic	MedinfoCZ@karopharma.com	+420-602 290 022
Denmark	MedinfoDK@karopharma.com
Estonia	MedinfoEE@karopharma.com
Finland	MedinfoFI@karopharma.com
France	MedinfoFR@karopharma.com	+33 1 81 79 38 34
Germany	MedinfoDE@Karopharma.com	0049 711 699 720 365
Greece	MedinfoGR@karopharma.com	302 103 511 771
Hungary	MedinfoHU@karopharma.com	36 1 3187160
Iceland	MedinfoIS@karopharma.com	5 222 900
Italy	MedinfoIT@karopharma.com
Ireland	MedinfoIE@karopharma.com	+44 (0) 1628 531171
Lithuania	MedinfoLT@karopharma.com
Latvia	MedinfoLV@karopharma.com	+371 2 9865787
Luxemburg	MedinfoLU@karopharma.com	+32 474 60 70 11
Malta	Medinfo@karopharma.com
Netherlands	MedinfoNL@karopharma.com	+32 474 60 70 11
Norway	MedinfoNO@karopharma.com	+46 (0) 101819102
Poland	MedinfoPL@karopharma.com	0-0-800-141-0269
Portugal	MedinfoPT@karopharma.com	+351 212 697 912
Romania	MedinfoRO@karopharma.com
Slovakia	MedinfoSK@karopharma.com	+420-602 290 022
Spain	MedinfoES@karopharma.com	+34 652 351 538
Sweden	MedinfoSE@karopharma.com	010-1805515
Switzerland	MedinfoCH@karopharma.com	+41 61 465 70 40
United Kingdom	MedinfoUK@karopharma.com	+44 (0) 1628 531171

Please note, we can only respond to Karo Pharma’s product-specific question.

Karo Pharma’s Global Patient Safety department work continuously with identifying, analysing, monitoring, and reporting potential side-effects or other potential risks on our medicinal products during their entire lifecycle to ensure that the benefit always outweigh the risk. Medicinal products are also monitored by Competent Authorities world-wide.

The purpose of the continuous safety monitoring is to discover any medicine-related problem, such as unexpected adverse events / side effects or changes in frequency of a known adverse events / side effects to continuously increase our knowledge, promote safe and effective use of our medicinal products, and to provide timely information to patients, healthcare professionals and the public

To report an adverse event / side effect/ Other safety information associated with the use of a Karo Medicinal Product, please contact the national Health Authority in the country of your residence, or contact your local Karo Pharma office, according to below Table I- Local Karo Pharma Office- Pharmacovigilance Contacts:

Adverse Event / Side-effect:

An Adverse Event is an untoward medical occurrence or a deterioration of a pre-existing medical condition after or during exposure to a Medicinal Product, regardless if a causal relationship has been assessed or not.

An adverse event can therefore be any unfavourable and unintended sign (e.g. an abnormal laboratory finding or electrocardiogram changes), symptom (e.g. rash, nausea, diarrhoea), or disease (e.g. hypothyroidism, anaemia, psoriasis) temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.

Other Safety Information we for example collect is Interactions, Off-label use, Overdose and if our Medicinal Product has been used during Pregnancy.

Territory	Email	Phone number
Austria	PVAT@karopharma.com	0049 711 699 720 365
Belgium	PVBE@Karopharma.com	+32 474 60 70 11
Bulgaria	PVBG@karopharma.com	+359 2 9156 135
Chech Republic	PVCZ@karopharma.com	+420-602 290 022
Denmark	PVDK@karopharma.com	+46 8 124 106 48
Estonia	PVEE@karopharma.com
Finland	PVFI@karopharma.com	+358 9 42411468
France	PVFR@karopharma.com	+33 1 81 79 38 34
Germany	PVDE@karopharma.com	0049 711 699 720 365
Greece	PVGR@karopharma.com	302 103 511 771
Hungary	PVHU@karopharma.com	36 1 3187160
Iceland	PVIS@karopharma.com	5222900
Italy	PVIT@karopharma.com
Ireland	PVIE@karopharma.com	+44 (0) 1628 531171
Lithuania	PVLT@karopharma.com
Latvia	PVLV@karopharma.com	37129865787
Luxemburg	PVLU@karopharma.com	+32 474 60 70 11
Malta	pv@karopharma.com
Netherlands	PVNL@karopharma.com	+32 474 60 70 11
Norway	PVNO@karopharma.com	+46 8 124 106 48
Poland	PVPL@karopharma.com	0-0-800-141-0269
Portugal	PVPT@Karopharma.com	351 212 697 912
Romania	PVRO@karopharma.com
Slovakia	PVSK@karopharma.com	+420-602 290 022
Spain	PVES@karopharma.com	+34 652 351 538
Sweden	PVSE@karopharma.com	+46 8 124 106 48
Switzerland	PVCH@karopharma.com	+41 61 465 70 40
United Kingdom	PVUK@karopharma.com	+44 (0) 1628 531171

We are committed to collect, analyse and react upon any new information about the benefits and risks of our Products.

If possible, we may contact you to find out more details or ask for clarification.

DPN

In order to handle your request, complaint or adverse event report, it is required according to pharmacovigilance legislation that Karo Pharma AB (“Karo Pharma”) register and process the personal data that you have provided to us.

The information you share with us will be protected and kept confidential in line with applicable laws, regulations, local legislations, and Karo Pharma data protection processes. More detailed information regarding the processing of your personal Information is available at https://www.karopharma.com/privacy-policy-com/

To report a Product Quality Complaint associated with the use of a Karo Product, please contact your nearest pharmacy.