ARICEPT 10 Milligram Film Coated Tablet

Ireland - English - HPRA (Health Products Regulatory Authority)

Buy It Now

Active ingredient:
DONEPEZIL HYDROCHLORIDE
Available from:
Clear Pharmacy
ATC code:
N06DA02
INN (International Name):
DONEPEZIL HYDROCHLORIDE
Dosage:
10 Milligram
Pharmaceutical form:
Film Coated Tablet
Prescription type:
Product subject to prescription which may not be renewed (A)
Therapeutic area:
Anticholinesterases
Authorization status:
Authorised
Authorization number:
PPA1596/047/002
Authorization date:
2011-06-23

Package leaflet: Information for the user

ARICEPT® 5 mg Film Coated Tablets

ARICEPT® 10 mg Film Coated Tablets

(Donepezil Hydrochloride)

Read all of this leaflet carefully before you start taking 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 doctor or pharmacist.

This medicine has been prescribed for you only. Do not pass it on to

others. It may harm them, even if their signs of illness are the same as

yours.

If you get any of the side effects talk to your doctor or pharmacist.

This includes any side possible effects not listed in this leaflet. See

section 4.

What is in this leaflet

1. What ARICEPT is and what it is used for

2. What you need to know before you take ARICEPT

3. How to take ARICEPT

4. Possible side effects

5. How to store ARICEPT

6. Contents of the pack and other information

1. What ARICEPT is and what it is used for

ARICEPT contains the active substance donepezil hydrochloride.

ARICEPT (donepezil hydrochloride) belongs to a group of medicines

called acetylcholinesterase inhibitors.

Donepezil increases the levels of a substance (acetylcholine) in the brain

involved in memory function by slowing down the break down of

acetylcholine.

It is used to treat the symptoms of dementia in people diagnosed as

having mild and moderately severe Alzheimer’s disease. The symptoms

include increasing memory loss, confusion and behavioural changes. As

a result, sufferers of Alzheimer’s disease find it more and more difficult

to carry out their normal daily activities.

ARICEPT is for use in adult patients only.

2. What you need to know before you take ARICEPT

Do not take ARICEPT

if you are allergic to donepezil hydrochloride, or to piperidine

derivatives, or any of the other ingredients of this medicine (listed in

section 6)

Warnings and precautions

Talk to your doctor or pharmacist before taking ARICEPT if you have or

have had:

stomach or duodenal ulcers

seizures (fits) or convulsions

a heart condition (irregular or very slow heart beat)

asthma or other long term lung disease

liver problems or hepatitis

difficulty passing urine or mild kidney disease

Also tell your doctor if you are pregnant or think you might be pregnant.

Children and adolescents

ARICEPT is not recommended for use in children and adolescents

(younger than 18 years of age).

Other medicines and ARICEPT

Tell your doctor or pharmacist if you are taking, have recently taken, or

might take any other medicines. This includes medicines that your

doctor has not prescribed for you but which you have bought yourself

from a chemist/pharmacist. It also applies to medicines you may take

sometime in the future if you continue to take ARICEPT. This is

because these medicines may weaken or strengthen the effects of

ARICEPT.

In particular it is important to tell your doctor if you are taking any of

the following types of medicines:

other Alzheimer’s disease medicines, e.g. galantamine

pain killers or treatment for arthritis e.g. aspirin, non-steroidal anti-

inflammatory (NSAID) drugs such as ibuprofen, or diclofenac

sodium

anticholinergics medicines, e.g. tolterodine

antibiotics e.g. erythromycin, rifampicin

anti-fungal medicine e.g. ketoconazole

anti-depressants e.g. fluoxetine

anticonvulsants e.g. phenytoin, carbamazepine

medication for a heart condition e.g. quinidine, beta-blockers

(propanolol and atenolol)

muscle relaxants e.g. diazepam, succinylcholine

general anaesthetic

medicines obtained without a prescription e.g. herbal remedies

If you are going to have an operation that requires you to have a general

anaesthetic, you should tell your doctor and the anaesthetist that you are

taking ARICEPT. This is because your medicine may affect the amount

of anaesthetic needed.

ARICEPT can be used in patients with kidney disease or mild to

moderate liver disease. Tell your doctor first if you have kidney or liver

disease. Patients with severe liver disease should not take ARICEPT.

Tell your doctor or pharmacist the name of your caregiver. Your

caregiver will help you to take your medicine as it is prescribed.

ARICEPT with food, drink and alcohol

Food will not influence the effect of ARICEPT.

ARICEPT should not be taken with alcohol because alcohol may change

its effect.

Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are

planning to have a baby, ask your doctor or pharmacist for advice before

taking any medicine.

ARICEPT should not be used while breastfeeding.

Driving and using machines

Alzheimer’s disease may impair your ability to drive or operate

machinery and you must not perform these activities unless your doctor

tells you that it is safe to do so.

Also, your medicine can cause tiredness, dizziness and muscle cramp.

If you experience any of these effects you must not drive or operate

machinery.

ARICEPT contains lactose

If you have been told by your doctor that you have intolerance to some

sugars, you should contact your doctor before taking ARICEPT.

3. How to take ARICEPT

How much ARICEPT should you take?

Always take this medicine exactly as your doctor or pharmacist has told

you. Check with your doctor or pharmacist if you are not sure. Initially,

the recommended dose is 5 mg (one white tablet) every night. After one

month, your doctor may tell you to take 10 mg (one yellow tablet) every

night.

The tablet strength you will take may change depending on the length of

time you have been taking the medicine and on what your doctor

recommends. The maximum recommended dose is 10 mg each night.

Do not alter the dose yourself without your doctor’s advice.

How to take your medicine

Swallow your ARICEPT tablet with a drink of water before you go to

bed at night.

Use in Children and adolescents

ARICEPT is not recommended for use in children and adolescents

(younger than 18 years of age).

If you take more ARICEPT than you should

Contact your doctor or the nearest hospital emergency department

immediately if you take more of the medicine than you should. Take this

leaflet and any remaining tablets with you.

Overdose symptoms may include feeling and being sick, drooling,

sweating, slow heart rate, low blood pressure (light-headedness or

dizziness when standing), breathing problems, losing consciousness and

seizures (fits) or convulsions.

If you forget to take ARICEPT

If you forget to take your medicine, take the next dose at the usual time.

Do not take a double dose to make up for a forgotten tablet.

If you forget to take your medicine for more than one week, call your

doctor before taking any more medicine.

C-PILARICEPT (CZ) V4

If you stop taking ARICEPT

Do not stop taking the tablets unless told to do so by your doctor. If you

stop taking ARICEPT, the benefits of your treatment will gradually fade

away.

If you have any further questions on the use of this medicine, ask your

doctor or pharmacist.

How long should you take ARICEPT?

Your doctor or pharmacist will advise you on how long you should

continue to take your tablets. You will need to see your doctor from time

to time to review your treatment and assess your symptoms.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not

everybody gets them.

The following side effects have been reported by people taking ARICEPT.

Tell your doctor if you have any of these effects while you are taking

ARICEPT.

Serious side effects:

You must tell your doctor immediately if you notice these serious side

effects mentioned. You may need urgent medical treatment.

liver damage e.g. hepatitis. The symptoms of hepatitis are feeling or

being sick, loss of appetite, feeling generally unwell, fever, itching,

yellowing of the skin and eyes, and dark coloured urine (may affect

up to 1 in 1,000 people).

stomach or duodenal ulcers. The symptoms of ulcers are stomach

pain and discomfort (indigestion) felt between the navel and the

breast bone (may affect up to 1 in 100 people).

bleeding in the stomach or intestines. This may cause you to pass

black tar like stools or visible blood from the rectum (may affect up

to 1 in 100 people).

seizures (fits) or convulsions (may affect up to 1 in 100 people).

fever with muscle stiffness, sweating or a lowered level of

consciousness (a disorder called “Neuroleptic Malignant

Syndrome”) (may affect up to 1 in 10,000 people).

Muscle weakness, tenderness or pain and particularly, if at the same

time, you feel unwell, have a high temperature or have dark urine.

They may be caused by an abnormal muscle breakdown which can

be life threatening and lead to kidney problems (a condition called

rhabdomyolysis) (may affect up to 1 in 10000 people)

Very common side effects (may affect more than 1 in 10 people)

diarrhoea

feeling sick

headaches

Common side effects (may affect up to 1 in 10 people)

muscle cramp

tiredness

difficulty in sleeping (insomnia)

the common cold

loss of appetite

hallucinations (seeing or hearing things that are not really there)

unusual dreams including nightmares

agitation

aggressive behaviour

fainting

dizziness

stomach feeling uncomfortable

rash

itching

passing urine uncontrollably

pain

accidents (patients may be more prone to falls and accidental injury)

Uncommon side effects (may affect up to 1 in 100 people)

slow heart beat

salivary hypersecretion

Rare side effects (may affect up to 1 in 1000 people)

stiffness, shaking or uncontrollable movement especially of the face

and tongue but also of the limbs

Reporting of side effects

If you get any the side effects, talk to your doctor or pharmacist. This

includes any possible side effects not listed in this leaflet. You can also

report side effects directly via

HPRA Pharmacovigilance, Earlsfort Terrace, IRL - Dublin 2;

Tel: +353 1 6764971; Fax: +353 1 6762517.

Website: www.hpra.ie; E-mail: medsafety@hpra.ie.

By reporting side effects you can help provide more information on the

safety of this medicine.

5. How to store ARICEPT

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the

outer carton and blister (EXP). The expiry date refers to the last day of

that month.

Do not store this medicine above 30°C.

Do not throw away any medicines via wastewater or household waste.

Ask your pharmacist how to dispose of medicines you no longer use.

These measures will help to protect the environment.

6. Contents of the pack and other information

What ARICEPT contains

The active substance is donepezil hydrochloride. Each 5 mg tablet

contains 5 mg of donepezil hydrochloride and each 10 mg tablet

contains 10 mg of donepezil hydrochloride.

The other ingredients are lactose monohydrate, maize starch,

microcrystalline cellulose,

hydroxypropyl cellulose,

magnesium

stearate,

hypromellose

, talc, macrogol, and titanium dioxide (E171).

Additionally, the 10 mg tablet contains synthetic yellow iron oxide

(E172).

What ARICEPT looks like and contents of the pack

ARICEPT 5 mg film coated tablets are white, round tablets marked

‘ARICEPT’ on one side and '5' on the other.

ARICEPT 10 mg film coated tablets are yellow, round tablets

marked ‘ARICEPT’ on one side and '10' on the other.

ARICEPT is available in packs of 28 tablets.

Procured from within the EU by the Parallel Product Authorisation

Holder:

Clear Pharmacy, 157-173 Roden Street, Belfast BT12 5QA, UK.

Manufacturer:

Pfizer PGM, Pocé-sur-Cisse, France

Repackager:

Pharmaram Limited, Unit F4, Ivanhoe Business Park, Tom Bill Way,

Ashby de la Zouch, Leicestershire, LE65 2UY, UK.

This medicinal product is authorised in Czech Republic as Aricept.

Leaflet date: December 2016

20161215

Package leaflet: Information for the user

ARICEPT® 5 mg Film Coated Tablets

ARICEPT® 10 mg Film Coated Tablets

(Donepezil Hydrochloride)

Read all of this leaflet carefully before you start taking 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 doctor or pharmacist.

This medicine has been prescribed for you only. Do not pass it on to

others. It may harm them, even if their signs of illness are the same as

yours.

If you get any of the side effects talk to your doctor or pharmacist.

This includes any side possible effects not listed in this leaflet. See

section 4.

What is in this leaflet

1. What ARICEPT is and what it is used for

2. What you need to know before you take ARICEPT

3. How to take ARICEPT

4. Possible side effects

5. How to store ARICEPT

6. Contents of the pack and other information

1. What ARICEPT is and what it is used for

ARICEPT contains the active substance donepezil hydrochloride.

ARICEPT (donepezil hydrochloride) belongs to a group of medicines

called acetylcholinesterase inhibitors.

Donepezil increases the levels of a substance (acetylcholine) in the brain

involved in memory function by slowing down the break down of

acetylcholine.

It is used to treat the symptoms of dementia in people diagnosed as

having mild and moderately severe Alzheimer’s disease. The symptoms

include increasing memory loss, confusion and behavioural changes. As

a result, sufferers of Alzheimer’s disease find it more and more difficult

to carry out their normal daily activities.

ARICEPT is for use in adult patients only.

2. What you need to know before you take ARICEPT

Do not take ARICEPT

if you are allergic to donepezil hydrochloride, or to piperidine

derivatives, or any of the other ingredients of this medicine (listed in

section 6)

Warnings and precautions

Talk to your doctor or pharmacist before taking ARICEPT if you have or

have had:

stomach or duodenal ulcers

seizures (fits) or convulsions

a heart condition (irregular or very slow heart beat)

asthma or other long term lung disease

liver problems or hepatitis

difficulty passing urine or mild kidney disease

Also tell your doctor if you are pregnant or think you might be pregnant.

Children and adolescents

ARICEPT is not recommended for use in children and adolescents

(younger than 18 years of age).

Other medicines and ARICEPT

Tell your doctor or pharmacist if you are taking, have recently taken, or

might take any other medicines. This includes medicines that your

doctor has not prescribed for you but which you have bought yourself

from a chemist/pharmacist. It also applies to medicines you may take

sometime in the future if you continue to take ARICEPT. This is

because these medicines may weaken or strengthen the effects of

ARICEPT.

In particular it is important to tell your doctor if you are taking any of

the following types of medicines:

other Alzheimer’s disease medicines, e.g. galantamine

pain killers or treatment for arthritis e.g. aspirin, non-steroidal anti-

inflammatory (NSAID) drugs such as ibuprofen, or diclofenac

sodium

anticholinergics medicines, e.g. tolterodine

antibiotics e.g. erythromycin, rifampicin

anti-fungal medicine e.g. ketoconazole

anti-depressants e.g. fluoxetine

anticonvulsants e.g. phenytoin, carbamazepine

medication for a heart condition e.g. quinidine, beta-blockers

(propanolol and atenolol)

muscle relaxants e.g. diazepam, succinylcholine

general anaesthetic

medicines obtained without a prescription e.g. herbal remedies

If you are going to have an operation that requires you to have a general

anaesthetic, you should tell your doctor and the anaesthetist that you are

taking ARICEPT. This is because your medicine may affect the amount

of anaesthetic needed.

ARICEPT can be used in patients with kidney disease or mild to

moderate liver disease. Tell your doctor first if you have kidney or liver

disease. Patients with severe liver disease should not take ARICEPT.

Tell your doctor or pharmacist the name of your caregiver. Your

caregiver will help you to take your medicine as it is prescribed.

ARICEPT with food, drink and alcohol

Food will not influence the effect of ARICEPT.

ARICEPT should not be taken with alcohol because alcohol may change

its effect.

Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are

planning to have a baby, ask your doctor or pharmacist for advice before

taking any medicine.

ARICEPT should not be used while breastfeeding.

Driving and using machines

Alzheimer’s disease may impair your ability to drive or operate

machinery and you must not perform these activities unless your doctor

tells you that it is safe to do so.

Also, your medicine can cause tiredness, dizziness and muscle cramp.

If you experience any of these effects you must not drive or operate

machinery.

ARICEPT contains lactose

If you have been told by your doctor that you have intolerance to some

sugars, you should contact your doctor before taking ARICEPT.

3. How to take ARICEPT

How much ARICEPT should you take?

Always take this medicine exactly as your doctor or pharmacist has told

you. Check with your doctor or pharmacist if you are not sure. Initially,

the recommended dose is 5 mg (one white tablet) every night. After one

month, your doctor may tell you to take 10 mg (one yellow tablet) every

night.

The tablet strength you will take may change depending on the length of

time you have been taking the medicine and on what your doctor

recommends. The maximum recommended dose is 10 mg each night.

Do not alter the dose yourself without your doctor’s advice.

How to take your medicine

Swallow your ARICEPT tablet with a drink of water before you go to

bed at night.

Use in Children and adolescents

ARICEPT is not recommended for use in children and adolescents

(younger than 18 years of age).

If you take more ARICEPT than you should

Contact your doctor or the nearest hospital emergency department

immediately if you take more of the medicine than you should. Take this

leaflet and any remaining tablets with you.

Overdose symptoms may include feeling and being sick, drooling,

sweating, slow heart rate, low blood pressure (light-headedness or

dizziness when standing), breathing problems, losing consciousness and

seizures (fits) or convulsions.

If you forget to take ARICEPT

If you forget to take your medicine, take the next dose at the usual time.

Do not take a double dose to make up for a forgotten tablet.

If you forget to take your medicine for more than one week, call your

doctor before taking any more medicine.

<INTERNAL CODE> (CZ) V4

If you stop taking ARICEPT

Do not stop taking the tablets unless told to do so by your doctor. If you

stop taking ARICEPT, the benefits of your treatment will gradually fade

away.

If you have any further questions on the use of this medicine, ask your

doctor or pharmacist.

How long should you take ARICEPT?

Your doctor or pharmacist will advise you on how long you should

continue to take your tablets. You will need to see your doctor from time

to time to review your treatment and assess your symptoms.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not

everybody gets them.

The following side effects have been reported by people taking ARICEPT.

Tell your doctor if you have any of these effects while you are taking

ARICEPT.

Serious side effects:

You must tell your doctor immediately if you notice these serious side

effects mentioned. You may need urgent medical treatment.

liver damage e.g. hepatitis. The symptoms of hepatitis are feeling or

being sick, loss of appetite, feeling generally unwell, fever, itching,

yellowing of the skin and eyes, and dark coloured urine (may affect

up to 1 in 1,000 people).

stomach or duodenal ulcers. The symptoms of ulcers are stomach

pain and discomfort (indigestion) felt between the navel and the

breast bone (may affect up to 1 in 100 people).

bleeding in the stomach or intestines. This may cause you to pass

black tar like stools or visible blood from the rectum (may affect up

to 1 in 100 people).

seizures (fits) or convulsions (may affect up to 1 in 100 people).

fever with muscle stiffness, sweating or a lowered level of

consciousness (a disorder called “Neuroleptic Malignant

Syndrome”) (may affect up to 1 in 10,000 people).

Muscle weakness, tenderness or pain and particularly, if at the same

time, you feel unwell, have a high temperature or have dark urine.

They may be caused by an abnormal muscle breakdown which can

be life threatening and lead to kidney problems (a condition called

rhabdomyolysis) (may affect up to 1 in 10000 people)

Very common side effects (may affect more than 1 in 10 people)

diarrhoea

feeling sick

headaches

Common side effects (may affect up to 1 in 10 people)

muscle cramp

tiredness

difficulty in sleeping (insomnia)

the common cold

loss of appetite

hallucinations (seeing or hearing things that are not really there)

unusual dreams including nightmares

agitation

aggressive behaviour

fainting

dizziness

stomach feeling uncomfortable

rash

itching

passing urine uncontrollably

pain

accidents (patients may be more prone to falls and accidental injury)

Uncommon side effects (may affect up to 1 in 100 people)

slow heart beat

salivary hypersecretion

Rare side effects (may affect up to 1 in 1000 people)

stiffness, shaking or uncontrollable movement especially of the face

and tongue but also of the limbs

Reporting of side effects

If you get any the side effects, talk to your doctor or pharmacist. This

includes any possible side effects not listed in this leaflet. You can also

report side effects directly via

HPRA Pharmacovigilance, Earlsfort Terrace, IRL - Dublin 2;

Tel: +353 1 6764971; Fax: +353 1 6762517.

Website: www.hpra.ie; E-mail: medsafety@hpra.ie.

By reporting side effects you can help provide more information on the

safety of this medicine.

5. How to store ARICEPT

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the

outer carton and blister (EXP). The expiry date refers to the last day of

that month.

Do not store this medicine above 30°C.

Do not throw away any medicines via wastewater or household waste.

Ask your pharmacist how to dispose of medicines you no longer use.

These measures will help to protect the environment.

6. Contents of the pack and other information

What ARICEPT contains

The active substance is donepezil hydrochloride. Each 5 mg tablet

contains 5 mg of donepezil hydrochloride and each 10 mg tablet

contains 10 mg of donepezil hydrochloride.

The other ingredients are lactose monohydrate, maize starch,

microcrystalline cellulose,

hydroxypropyl cellulose,

magnesium

stearate,

hypromellose

, talc, macrogol, and titanium dioxide (E171).

Additionally, the 10 mg tablet contains synthetic yellow iron oxide

(E172).

What ARICEPT looks like and contents of the pack

ARICEPT 5 mg film coated tablets are white, round tablets marked

‘ARICEPT’ on one side and '5' on the other.

ARICEPT 10 mg film coated tablets are yellow, round tablets

marked ‘ARICEPT’ on one side and '10' on the other.

ARICEPT is available in packs of 28 tablets.

Procured from within the EU by the Parallel Product Authorisation

Holder:

Clear Pharmacy, 157-173 Roden Street, Belfast BT12 5QA, UK.

Manufacturer:

Pfizer PGM, Pocé-sur-Cisse, France

Repackager:

Cast Healthcare Limited, 5-7 Tobermore Road, Draperstown

BT45 7AG, UK.

This medicinal product is authorised in Czech Republic as Aricept.

Leaflet date: December 2016

20161215

Summary of Product Characteristics

1 NAME OF THE MEDICINAL PRODUCT

Aricept 10mg Film-coated Tablets

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

10 mg donepezil hydrochloride tablets each containing 9.12 mg of donepezil free base.

Excipient: lactose monohydrate 174.33 mg per tablet.

For full list of excipients, see section 6.1.

3 PHARMACEUTICAL FORM

Film-coated Tablet

Product imported from the Czech Republic:

Yellow round, biconvex tablets embossed ‘ARICEPT’ on one side and ‘10’ on the other side.

4 CLINICAL PARTICULARS

As per PA0822/002/002

5 PHARMACOLOGICAL PROPERTIES

As per PA0822/002/002

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Lactose monohydrate

Maize starch

Microcrystalline cellulose

Hyprolose

Magnesium stearate

film coating

Talc

Macrogol 8000

Hypromellose

Titanium dioxide (E171)

Yellow iron oxide (E172)

6.2 Incompatibilities

Not applicable

6.3 Shelf life

The shelf-life expiry date of this product shall be the date shown on the container and outer packaging of the product on

the market in the country of origin.

H

e

a

l

t

h

P

r

o

d

u

c

t

s

R

e

g

u

l

a

t

o

r

y

A

u

t

h

o

r

i

t

y

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

D

a

t

e

P

r

i

n

t

e

d

1

1

/

0

1

/

2

0

1

7

C

R

N

2

1

8

7

2

5

5

p

a

g

e

n

u

m

b

e

r

:

1

6.4 Special precautions for storage

Do not store above 30°C.

6.5 Nature and contents of container

Blisters in cardboard cartons of 28 tablets.

6.6 Special precautions for disposal of a used medicinal product or waste materials derived from

such medicinal product and other handling of the product

No special requirements

7 PARALLEL PRODUCT AUTHORISATION HOLDER

Clear Pharmacy

157-173 Roden Street

Belfast BT12 5QA

United Kingdom

8 PARALLEL PRODUCT AUTHORISATION NUMBER

PPA1596/047/002

9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

Date of first authorisation: 23

June 2011

10 DATE OF REVISION OF THE TEXT

January 2017

H

e

a

l

t

h

P

r

o

d

u

c

t

s

R

e

g

u

l

a

t

o

r

y

A

u

t

h

o

r

i

t

y

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

_

D

a

t

e

P

r

i

n

t

e

d

1

1

/

0

1

/

2

0

1

7

C

R

N

2

1

8

7

2

5

5

p

a

g

e

n

u

m

b

e

r

:

2

Similar products

Search alerts related to this product

View documents history

Share this information