NUEDEXTA

Krajina: Izrael

Jazyk: angličtina

Zdroj: Ministry of Health

Aktívna zložka:

DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE

Dostupné z:

MEDISON PHARMA LTD

ATC kód:

C01BA01

Forma lieku:

CAPSULES

Zloženie:

QUINIDINE SULFATE 10 MG; DEXTROMETHORPHAN HYDROBROMIDE 20 MG

Spôsob podávania:

PER OS

Typ predpisu:

Required

Výrobca:

AVANIR PHARMACEUTICALS, USA

Terapeutické oblasti:

QUINIDINE

Terapeutické indikácie:

For the treatment of Pseudobulbar Affect (PBA) .

Dátum Autorizácia:

2018-05-31

Príbalový leták

PATIENT LEAFLET IN ACCORDANCE WITH THE PHARMACISTS’
REGULATIONS (PREPARATIONS) 1986
This medicine is dispensed with a doctor’s prescription only
NUEDEXTA
CAPSULES
ACTIVE INGREDIENTS: DEXTROMETHORPHAN HYDROBROMIDE
20 MG AND QUINIDINE SULFATE 10 MG
INACTIVE
INGREDIENTS:
See
the
section
“Important
information about some of this medicine’s ingredients”
and section 6 “Additional information”.
READ THE ENTIRE LEAFLET CAREFULLY BEFORE YOU START USING
THIS MEDICINE. This leaflet contains concise information
about this medicine.
If you have any further questions, ask your doctor or
pharmacist.
This medicine has been prescribed to treat your illness.
Do not pass it on to others. It may harm them, even if it
seems to you that their illness is similar.
1.
WHAT IS THIS MEDICINE INTENDED FOR?
Nuedexta is intended for the treatment of pseudobulbar
affect (PBA), a secondary effect to a variety of neurological
disorders,
unrelated
to
each
other,
characterized
by
involuntary, sudden and frequent events of crying and/or
laughing. PBA events are characterized by their occurrence
being unrelated to the underlying emotional state of the
patient.
THERAPEUTIC GROUP: medicinal products acting on the
nervous
system.
2.
BEFORE USING THIS MEDICINE
DO NOT USE THIS MEDICINE:
If you are sensitive (allergic) to the active ingredients
or to any of the other ingredients that this medicine
contains (See section 6).
In certain cases of cardiovascular disorders and in
patients with heart failure.
If you have previously suffered from thrombocytopenia
caused by using Nuedexta, quinine, mefloquine or
quinidine.
If you have previously suffered from hepatitis.
If you have previously suffered from bone marrow
suppression; or lupus-like symptoms.
In combination therapy with medicines containing
quinidine, quinine, mefloquine.
In
combination
therapy
with
monoamine
oxidase
inhibitors
or
if
you
have
taken
medicines
in
the
monoamine oxidase inhibitor class within the 14 days
preceding this treatment. In addition, you should wait
14 days after you

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