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LORATADINE STADA 10 mg FILM-COATED TABLETS

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About the medicine

How to use LORATADINE STADA 10 mg FILM-COATED TABLETS

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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.

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Introduction

Package Leaflet: Information for the User

LORATADINA STADA 10 mg film-coated tablets EFG

Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.

  • Keep this package leaflet, as you may need to read it again.
  • If you have any questions, consult your doctor or pharmacist.
  • This medication has been prescribed to you only and you should not give it to others, even if they have the same symptoms as you, as it may harm them.
  • If you experience side effects, consult your doctor or pharmacist, even if they are not listed in this package leaflet. See section 4.

Contents of the package leaflet

  1. What is Loratadina STADA and what is it used for
  2. What you need to know before taking Loratadina STADA
  3. How to take Loratadina STADA
  4. Possible side effects
  5. Storage of Loratadina STADA
  6. Contents of the pack and further information

1. What is Loratadina STADA and what is it used for

Loratadina STADA belongs to a class of medications known as antihistamines.

Loratadina STADA relieves the symptoms associated with allergic rhinitis (such as sneezing, runny or itchy nose and irritation or itching of the eyes).

Loratadina STADA can also be used to help relieve the symptoms of urticaria (such as itching, redness, and the number and size of skin wheals).

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2. What you need to know before taking Loratadina STADA

Do not take Loratadina STADA:

  • If you are allergic to loratadine or any of the other components of this medication (listed in section 6).

Warnings and precautions

Consult your doctor or pharmacist before starting to take Loratadina STADA.

  • If you have severe liver disease (see section 3, "How to take Loratadina STADA").
  • If you are going to undergo any type of skin allergy test. Do not take Loratadina STADA for 2 days before the test, as this medication may alter the results.

Use of Loratadina STADA with other medications

Tell your doctor or pharmacist if you are taking, have recently taken, or may take any other medication.

No interactions with Loratadina STADA and other medications are known.

Taking Loratadina STADA with food and drinks

Loratadina STADA can be taken with or without food.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.

Loratadina STADA is not recommended if you are pregnant or breastfeeding.

Driving and using machines

At normal doses, Loratadina STADA does not affect the ability to drive or use machines.

If you notice symptoms of drowsiness, do not drive or use machines, and avoid performing tasks that require special attention until you know how you tolerate the medication.

Loratadina STADA contains lactose

This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.

Medicine questions

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3. How to take Loratadina STADA

Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

Remember to take your medication.

Your doctor will indicate the duration of your treatment with Loratadina STADA. Do not stop treatment before.

Adults and children over 2 years of age with a weight over 30 kg:

Take one tablet (10 mg) once a day.

Patients with severe liver problems with a weight over 30 kg:

Take one tablet (10 mg) once a day, every other day.

Loratadina STADA 10 mg film-coated tablets are not suitable for:

  • administration of doses less than 10 mg.
  • administration in patients with a weight less than 30 kg.
  • patients who have difficulty swallowing.

Loratadina STADA is not recommended for children under 2 years of age.

If you take more Loratadina STADA than you should

If you have taken more Loratadina STADA than you should, consult your doctor or pharmacist immediately.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

If you forget to take Loratadina STADA

If you forget to take your dose on time, take it as soon as possible, and then return to your usual dosing schedule

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

If you have any further questions about the use of this medication, ask your doctor or pharmacist.

4. Possible side effects

Like all medications, this medication can cause side effects, although not everyone gets them.

The most frequently reported side effects (less than 1 in 10 patients but more than 1 in 100 patients) include drowsiness, headache, nervousness, fatigue, increased appetite, and difficulty sleeping.

Very rare side effects (less than 1 in 10,000 patients) have been reports of severe allergic reactions, dizziness, irregular or rapid heartbeats, nausea (vomiting), dry mouth, upset stomach, liver problems, hair loss, skin rash, fatigue, and convulsions.

Frequency not known (frequency cannot be estimated from available data):

Weight gain

Reporting side effects

If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this package leaflet. You can also report them through the Spanish Medication Surveillance System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medication.

5. Storage of Loratadina STADA

Keep out of sight and reach of children.

No special storage conditions are required.

Do not use Loratadina STADA after the expiration date stated on the packaging, after CAD. The expiration date is the last day of the month indicated.

Do not use Loratadina STADA if you notice any change in the appearance of the tablet.

Medications should not be disposed of through wastewater or household waste. Deposit the packaging and any unused medication in the pharmacy's SIGRE collection point. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medication. This will help protect the environment.

6. Contents of the pack and further information

Composition of Loratadina STADA

  • The active ingredient is loratadine. Each film-coated tablet contains 10 mg of loratadine.
  • The other ingredients are: lactose monohydrate, microcrystalline cellulose, corn starch, pregelatinized corn starch, colloidal silicon dioxide, magnesium stearate, hypromellose, macrogol 400, macrogol 6000, carnauba wax, and talc.

Appearance of the product and contents of the pack

Loratadina STADA is presented in the form of film-coated tablets, white, round, biconvex, with a score line on one side and the inscription "LR 10" on the other. Each pack contains 20 tablets in blisters.

Marketing authorization holder and manufacturer

Marketing authorization holder:

Laboratorio STADA, S.L.

Frederic Mompou, 5

08960 San Just Desvern (Barcelona)

[email protected]

Manufacturer:

Neuraxpharm Pharmaceuticals, S.L.

Avda. Barcelona, 69

08970 San Joan Despí

Date of the last revision of this package leaflet:December 2017

Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/

Online doctors for LORATADINE STADA 10 mg FILM-COATED TABLETS

Discuss questions about LORATADINE STADA 10 mg FILM-COATED TABLETS, including use, safety considerations and prescription review, subject to medical assessment and local regulations.

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Tarek Agami

General medicine 11 years exp.

Dr. Tarek Agami is a general practitioner registered in both Portugal and Israel, with broad experience in family and preventive medicine. He offers online consultations for adults and children, providing personalised support for primary care needs, chronic disease management, and everyday health concerns.

Dr. Agami received clinical training and worked in leading medical institutions in Israel (Kaplan Medical Center, Barzilai Medical Center, Wolfson Medical Center) and Portugal (European Healthcare City, Viscura Internacional, Hospital Dr. José Maria Grande, Hospital Vila Franca de Xira). His approach combines international medical standards with individualised attention to each patient.

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Dr. Agami provides medical support for patients using GLP-1 medications (such as Ozempic or Mounjaro) as part of a weight loss strategy. He offers individualised treatment planning, regular follow-up, dose adjustment, and advice on combining medication with sustainable lifestyle changes. Consultations follow the medical standards accepted in Portugal and Israel.

Dr. Agami is committed to evidence-based, patient-centred care, ensuring that each person receives trusted medical support tailored to their health goals.

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Nuno Tavares Lopes

Family medicine 18 years exp.

Dr. Nuno Tavares Lopes is a licensed physician in Portugal with 17 years of experience in emergency medicine, family and general practice, and public health. He is the Director of Medical and Public Health Services at an international healthcare network and serves as an external consultant for the WHO and ECDC.

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Dr. Nuno Tavares Lopes provides medical support for patients using GLP-1 medications (Mounjaro, Wegovy, Ozempic, Rybelsus) as part of a weight loss strategy. He offers individualised treatment planning, regular follow-up, dose adjustment, and advice on combining medication with sustainable lifestyle changes. Consultations follow the medical standards accepted in Europe.

Dr. Lopes also provides interpretation of medical tests, follow-up care for complex patients, and multilingual support. Whether for urgent concerns or long-term care, he helps patients act with clarity and confidence.

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Anastasiia Shalko

Family medicine 13 years exp.

Dr. Anastasiia Shalko is a general practitioner with a background in both paediatrics and general medicine. She graduated from Bogomolets National Medical University in Kyiv and completed her paediatric internship at the P.L. Shupyk National Medical Academy of Postgraduate Education. After working as a paediatrician in Kyiv, she relocated to Spain, where she has been practising general medicine since 2015, providing care for both adults and children.

Her work focuses on urgent, short-term medical concerns – situations where patients need quick guidance, symptom assessment and clear next steps. She helps people understand whether their symptoms require in-person evaluation, home management or a change in treatment. Common reasons for booking an online consultation include:

  • acute respiratory symptoms (cough, sore throat, runny nose, fever)
  • viral illnesses such as colds and seasonal infections
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Dr. Shalko works specifically with urgent and short-term problems, providing practical recommendations and helping patients determine the safest next step. She explains symptoms clearly, guides patients through decision-making and offers straightforward medical advice for everyday acute issues.

She does not provide long-term management of chronic conditions, ongoing follow-up or comprehensive care plans for complex long-term illnesses. Her consultations are designed for acute symptoms, sudden concerns and situations where timely medical input is important.

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Tomasz Grzelewski

Dermatology 21 years exp.

Dr Tomasz Grzelewski is an MD, PhD specialist in allergy, paediatrics, general practice and sports medicine, with a clinical focus on dermatology, endocrinology, allergology and sports-related health. He has more than 20 years of clinical experience and completed his medical training at the Medical University of Łódź, where he defended his PhD thesis with distinction. His doctoral research was recognised by the Polish Society of Allergology for its innovative contribution to the field. Throughout his career, he has gained extensive expertise in diagnosing and managing a wide range of allergic and paediatric conditions, including modern allergen desensitisation techniques.

For five years, Dr Grzelewski served as the Head of two paediatric departments in Poland, managing complex clinical cases and leading multidisciplinary teams. He also worked in medical centres in the United Kingdom, gaining experience across both primary care and specialist environments. With over a decade of telemedicine experience, he has provided online consultations across Europe and is valued for his clear, structured and evidence-based medical guidance.

Dr Grzelewski is actively involved in clinical programmes focused on modern anti-allergic therapies. As a Principal Investigator, he leads research projects on sublingual and oral allergen desensitisation, supporting evidence-based progress in allergy treatment for both children and adults.

In addition to his background in allergology and paediatrics, he completed dermatology studies through the Cambridge Education Group (Royal College of Physicians of Ireland) and a Clinical Endocrinology course at Harvard Medical School. This advanced training enhances his ability to manage skin manifestations of allergies, atopic conditions, urticaria, endocrine-related symptoms and complex immunological reactions.

Patients commonly seek his care for:

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Dr Tomasz Grzelewski is known for his clear communication style, structured medical approach and ability to explain treatment options in a concise and accessible way. His multidisciplinary background across allergy, paediatrics, dermatology and endocrinology allows him to provide safe, up-to-date and comprehensive care for patients of all ages.
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Frequently Asked Questions

Is a prescription required for LORATADINE STADA 10 mg FILM-COATED TABLETS?
LORATADINE STADA 10 mg FILM-COATED TABLETS requires a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
What is the active substance in LORATADINE STADA 10 mg FILM-COATED TABLETS?
The active ingredient in LORATADINE STADA 10 mg FILM-COATED TABLETS is loratadine. This information helps identify medicines with the same composition but different brand names.
How much does LORATADINE STADA 10 mg FILM-COATED TABLETS cost in pharmacies?
The average pharmacy price for LORATADINE STADA 10 mg FILM-COATED TABLETS is around 3.11 EUR. Prices may vary depending on the manufacturer and dosage form.
Who manufactures LORATADINE STADA 10 mg FILM-COATED TABLETS?
LORATADINE STADA 10 mg FILM-COATED TABLETS is manufactured by Laboratorio Stada S.L.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of LORATADINE STADA 10 mg FILM-COATED TABLETS online?
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether LORATADINE STADA 10 mg FILM-COATED TABLETS is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
What are the alternatives to LORATADINE STADA 10 mg FILM-COATED TABLETS?
Other medicines with the same active substance (loratadine) include CIVERÁN 10 mg FILM-COATED TABLETS, CLARITYNE 10 mg TABLETS, LORATADINE ALMUS 10 mg TABLETS. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
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