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Loiler tablets, 20 pcs

Loiler tablets, 20 pcs

For the treatment of complaints with allergic conditional nose (e.g., hay fever) and chronic, idiopathic urticaria (hives of unknown cause).

Manufacturers: DERMAPHARM AG

PZN: 01827598

Dosage: Tabletten

Content: 20 St

Reward Points: 54

Availability: Out of stock

$16.11

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Loiler tablets, 20 pcs

Instructions for use for Loiler tablets, 20 pcs

Instructions for use for: LOORADERM Tablets, 20 pcs

Important notes (compulsory information):

Loraderm 10 mg tablets.
Active ingredient: loratadine. Areas of application: Used to treat the complaints with allergic conditional nose (e.g., hay fever) and chronic, idiopathic urticaria (hives unknown cause.

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.


LEAFLET: INFORMATION FOR THE USER

LORADERM 10 mg tablets
Active ingredient: loratadin

Read the entire leaflet carefully before you start taking this medicine because it contains important information. Always take this medicine exactly as described in this leaflet or exactly as your doctor or pharmacist instructions.
  • Lift the package leaflet. You might want to read it again.
  • Ask your pharmacist if you need more information or advice.
  • If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not indicated in this leaflet. See section 4.
  • If you do not feel better or even worse after 7 days, contact your doctor.


What is in this leaflet:
  1. What is Loraderm and what is it used for?
  2. What should you consider before taking LORADERM?
  3. What is Loraderm taking?
  4. WHAT SIDE EFFECTS ARE POSSIBLE?
  5. How to keep latoraderm?
  6. Content of the pack and further information


1. What is loraderm and what is it used for?

LORADERM is part of the group of antihistamines. LOORADERM is used to treat the discomfort with allergic conditional nose (e.g. Hay fever) and chronic, idiopathic urticaria (Hesselucht Unknown Cause) used.

2. What should you consider before taking LORADERM?

LORADERM may not be taken if they are allergic to loratadine or one of the other ingredients of this medicine referred to in section 6.

Warnings and Precautions:
Please talk to your doctor or pharmacist before taking Loraderm:
  • if you suffer from a heavy hepatic impairment.
  • if you plan to carry out a skin test. The application of LOORADERM should be interrupted at least 48 hours prior to the implementation of skin tests, as antihistamines like loraderm otherwise prevent positive reactions to skin test.


Taking LORADERM along with other medicines:
Inform your doctor or pharmacist when taking other medicines, recently taken other medicines or intend to take other medicines. No interactions were described in the clinical trials carried out.

Taking LORADERM along with food and beverages:
The effect of alcohol is not enhanced by taking LORADERM.

Pregnancy and breast feeding period:
If you are pregnant or breastfeeding, or if you suspect to be pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this medicine. In animal experimental studies, no fruit harmful effects of Loratadine was found. In over 1000 Births after ingestion during pregnancy, there were no signs of damage to the unborn through loratadine. As a precautionary measure, the intake of LORADERM during pregnancy should still be avoided as much as possible. Loratadin goes into breast milk. Therefore, an intake of LORADERM in lactation is decreased.

Driving and ability to operate machines:
In some individuals, it can come in very rare cases to dizziness, which is affectedcan lead to the ability to drive or the ability to serve machines. It is therefore advisable to wait for your individual response to the revenue of LORADERM before leading a vehicle or serve machines.

LOORADERM contains lactose:
Please take LORADER only after consulting your doctor if you are familiar with any intolerance to certain sugars.

3. How to take LORADERM?

Always take this medicine exactly as described in this leaflet or just according to the consultation made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure. Please ask your doctor or pharmacist if you have the impression that the effect of LORADERM is too strong or too weak. The recommended dose is: adults and children over 12 years: 1-time daily 1 tablet LORADERM (corresponding to 10 mg loratadine). Children from 2 to 12 years: with a body weight of over 30 kg: 1-time daily 1 tablet LORADERM (corresponding to 10 mg loratadine). With a body weight of 30 kg and below: the tablet in the dose thickness of 10 mg is for children with a body weight under 30 kg not suitable. The effectiveness and safety of LORADERM in children under 2 years are not proven. Patients with heavy liver damage: It will be an initial dose of 1 Tablet Loraderm (corresponding to 10 mg loratadine) every other day in adults and recommended in children with a body weight over 30 kg. Dose adjustment in older patients or in patients with renal insufficiency is not required.

Type of application:
To take. The tablet can be taken independently of the meals.

If you take a greater amount of LORADERM than you should:
With a overdose of loratadine, drowsiness, accelerated heartbeat (tachycardia) and headache were described. If you have taken too many tablets LORADERM, please contact your doctor or pharmacist immediately. In the case of an overdose, a treatment-focused and supported and supported on the complaint must be initiated and to continue as long as necessary. In water-dissolved activated carbon can be administered. An stomach rinse can be considered. Loratadine is not removed by blood linen (hemodialysis) and it is not known if loratadine is excreted by peritoneal dialysis. After emergency treatment, the patient must continue to be under medical supervision.

If you forget to take LORADERM:
Do not take the double amount when you forget the previous taking. If you have forgotten the timely intake of a tablet, take it as soon as possible. Then continue as recommended.

If you cancel the intake of LORADERM:
Her illness could deteriorate.

If you have further questions about the application of this medicine, contact your doctor or pharmacist.

4. Which side effects are possible?

Like all medicines, this medicine can also have side effects, but they do not have to occur each other. The assessment of side effects is based on the following frequency information:

The frequency information on side effects is based on the following categories:
Very often: more than 1 treated from 10
Frequently: 1 to 10 treated from 100
Occasionally: 1 to 10 treated from 1 000
Rarely: 1 to 10 treated from 10 000
Very rare: less than 1 treated from 10 000
Not known: Frequency on the basis of the available data does not estimate.


Significantly side effects or characters to which you should pay attention and measures if they are affected by:
If you are of one of the successionnD Side effects are affected, do not take Loraderm further and look for your doctor as soon as possible.

Immune system:
Very rare: Hypersensitivity reactions (including quincke edema and anaphylaxis)

Nervous system:
Often: nervousness
Very rare: dizziness, cramps

Cardiovascular:
Very rare: accelerated heartbeat (tachycardia), palpitations or cardiac grids (palpitations)

Gastrointestinaltrakt:
Very rare: nausea, mouth dryness, gastric mucosal inflammation (Gastritis)

Liver and bile tract:
Very rare: hepatic impairment

Skin and subcutaneous tissue:
Very rare: rash, hair loss (alopecia)

General disorders:
Often: headache, fatigue, drowsiness
Occasionally: insomnia, appetite

Message of side effects:
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not indicated in this leaflet. You can also effectively effect the Federal Institute for Medicines and Medical Devices, Dept. Pharmacovigilance, Kurt-Georg-Kiesinger Allee 3, D-53175 Bonn, website: www.bfarm.de. By reporting side effects, you can help to provide more information about the security of this medicine.

5. How to keep LORADERM?

Keep this medicine inaccessible to children. You may not use this medicine after the expirable date used on the blister and the folding box according to "until" specified until ". The expiry date refers to the last day of the specified month.

6. Content of the pack and further information

What Loraderm contains:
The active ingredient is loratadine. A tablet contains 10 mg loratadine. The other ingredients are: lactose monohydrate, corn starch and magnesium stearate.

Like Loraderm looks and content of the pack:
LORADERM is a white tablet with fracture notch and is available in packs of 20 pieces, 50 pieces and 100 pieces.

Pharmaceutical entrepreneur:
Dermapharm AG
Lil-Dagover ring 7
82031 green forest
Tel: 089/641 86 0
Fax. 089/641 86 130
E-mail: [email protected]

Manufacturer:
MIBE GmbH medicine
Munich Straße 15
06796 Brehna
(a subsidiary of Dermapharm AG)

This leaflet was recently revised in February 2015.

Source: Information of the leaflet
Status: 08/2016

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.

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