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LAMBERTS DEVILS CLAW TABLETS

Active substance(s): DEVILS CLAW QUANTIFIED DRY EXTRACT

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LH3664 Devils Claw THR lft July2016 AW_Layout 1 28/07/2016 14:58 Page 1

®

Lamberts Devil’s Claw Tablets
Devil’s Claw Root Extract 450mg
8003

Patient Information Leaflet
Lamberts® Devil’s Claw Tablets
Please read this information carefully before
you start taking these tablets. It contains some
important information about this product. Keep
this leaflet with the tablets. You may want to
read it again or show it to your doctor,
pharmacist or qualified healthcare practitioner.

What is in this leaflet

• Are pregnant or breastfeeding
• Are allergic to Devil’s Claw or any of the
ingredients (see section 6)
• Are under the age of 18 years
Tell your doctor before taking this product
if you:
• Have heart problems and want to take this
product

1. What this product is and what it is used for
2. Before you take this product
3. How to take this product
4. Possible side effects
5. How to store this product
6. Further information

1. What this product is and what it is
used for
This product is a traditional herbal medicinal
product containing Devil’s Claw root extract.
Each film-coated tablet contains 450mg of
extract (as dry extract) from Devil’s Claw root
(Harpagophytum procumbens D.C. and/or
H.zeyheri L. Decne, radix) (Equivalent to
1575mg-2250mg of Devil’s Claw root).
Extraction Solvent Ethanol 60% v/v
Lamberts® Devil’s Claw is a traditional
herbal medicinal product used for the relief
of backache, rheumatic or muscular pain,
and general aches and pains in the
muscles and joints. This is based on
traditional use only.

2. Before you take this product
Do not take this product if you:
• Have ever had or have a stomach ulcer or
duodenal ulcer

Consult your doctor or qualified healthcare
practitioner if your:
• joint pain is accompanied by swelling of
the joint, redness or fever
• symptoms worsen or do not improve after
4 weeks
Driving or operating machines
This product may cause dizziness and
drowsiness. If this happens to you, do not
drive or use machines.

3. How to take this product
For oral use only
Adults and the elderly:
Take one tablet twice a day (in the morning and
in the evening). Tablets should be swallowed
whole with some water or other liquid.
Do not exceed the stated dose.
If you take too much of this product (overdose)
If you take more than the recommended dose,
speak to a doctor, pharmacist or qualified
healthcare practitioner and take this leaflet
with you.
If you forget to take this product
Continue to take your usual dose at the
usual time, it does not matter if you have
missed a dose.

LH3664 Devils Claw THR lft July2016 AW_Layout 1 28/07/2016 14:58 Page 2

After taking this product

6. Further information

You must speak to a qualified healthcare
practitioner if your symptoms worsen, if they
do not improve after four weeks, or if side
effects not mentioned in this leaflet occur.

Active Ingredient

4. Possible side effects
Like all medicines, this product can have
side-effects. These are listed below:
Digestive disorders - diarrhoea, feeling sick,
being sick, abdominal pains

Each film-coated tablet contains 450mg of
extract (as dry extract) from Devil’s Claw root
(Harpagophytum procumbens D.C. and/or
H.zeyheri L. Decne, radix) (Equivalent to
1575mg-2250mg
Devil’s
Claw
root).
Extraction Solvent: Ethanol 60% v/v.
This product also contains the following
ingredients:

-

Excipients in the extract: - Maltodextrin,
Silica Colloidal Anhydrous.

Skin disorders - allergic skin reactions such
as rash and itching

Tablet Core: Maltodextrin, Microcrystalline
Cellulose, Croscarmellose Sodium, Stearic
Acid, Magnesium Stearate, Colloidal
Anhydrous Silica.

Central nervous system
headache, dizziness

disorders

If any of the effects become troublesome or
if you experience any other unexpected
effects not listed in the leaflet, consult your
doctor or pharmacist.
Reporting of side effects
If you get any side effects, talk to your
doctor, pharmacist or nurse. This includes
any possible side effects not listed in the
package leaflet. You can also report side
effects directly via the Yellow Card Scheme
at www.mhra.gov.uk/yellowcard.
By reporting side effects you can help
provide more information on the safety of
this medicine.

5. How to store this product
Keep the tablets out of sight and reach
of children.
Keep your tablet in the packaging until it is
time to take them.
Do not store above 25°C. Store in the
original package.
Do not use Lamberts® Devil’s Claw tablets
after the expiry date which is stated on the
box and blister pack. The expiry date refers
to the last day of that month. Return any
out-of-date tablets to your pharmacist who
will dispose of them for you.

Coating: Hypromellose, Titanium Dioxide,
Copper Chlorophyllin, Glycerin
The tablets are green coated and oval shaped.
Each pack contains 30, 60 or 90 film coated
tablets.
Not all pack sizes may be marketed.
Traditional Registration holder for this product:
Lamberts Healthcare Ltd, 1 Lamberts Road,
Tunbridge Wells, Kent TN2 3EH.
Manufacturer of this product:
Thompson & Capper Ltd, Hardwick Road,
Astmoor, Runcorn, Cheshire WA7 1PH.
Traditional Herbal Registration Number:
THR 34425/0003
If you would like further information about
this product or would like a large print,
Braille or audio version of this leaflet please
contact:
Lamberts
Healthcare
Ltd,
1 Lamberts Road, Tunbridge Wells, Kent
TN2 3EH. Tel: 01892 554312.
This leaflet was revised in July 2016.
LK44-2

Certification Mark

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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