Leaflet: information for the user
Dosil 100 mg hard capsules
Doxiciclina
Read this leaflet carefully before you start taking the medicine, because it contains important information for you.
1. What is Dosil and what it is used for
2. What you need to know before starting to take Dosil
3. How to take Dosil
4. Possible side effects
5. Storage of Dosil
6. Contents of the pack and additional information
Dosilcontains doxiciclina, an antibiotic that belongs to a group called tetraciclinas.
Antibiotics are used to treat bacterial infections and do not work for viral infections.
It is essential to follow the instructions regarding dosage, administration interval, and treatment duration indicated by your doctor.
Do not store or use this medication. If you have leftover antibiotic after completing treatment, return it to the pharmacy for proper disposal. Do not dispose of medications through the drain or in the trash.
Dosil is indicated for:
Do not take Dosil
-If you are allergic to doxycycline, any other tetracycline, or any of the other components of this medication (listed in section 6).
-If you are using it together with methoxyflurane (a medication used for anesthesia), as it can cause severe kidney toxicity with fatal outcome.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Dosil:
-If during treatment with Dosil you notice abnormal headaches accompanied by dizziness, blurred vision, ringing in the ears, nausea, or vomiting, consult your doctor, as they may be symptoms of benign intracranial hypertension (a process affecting the brain due to an increase in pressure within the skull). In young children, it may cause fontanelle bulging (unossified space of the skull in young children). These alterations disappear when the treatment is interrupted,
-If you are taking a medication called isotretinoin, as taken together with Dosil it may cause benign intracranial hypertension,
Children
-Dosilshould not be used in children in the teething period (last half of pregnancy, infants, and children under 8 years old) because it may cause permanent tooth discoloration, as well as delayed bone development.
Use in children and adolescents
-In children under 8 years old, the use of Dosil is not recommended.
-In children over 8 years old and over 45 kg of weight, it is recommended to use the same dose as in adults, see section 3.
Taking Dosil with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Certain medications may interact with Dosil. In these cases, it may be necessary to change the dose or discontinue treatment with one of the medications. It is especially important to inform your doctor if you are using any of the following medications:
Taking Dosil with food, drinks, and alcohol
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
The use of Dosil during pregnancy is not recommended, as it may cause bone and tooth development disorders in the child. Your doctor will decide whether to use Dosil in these cases.
It is essential to use contraceptive methods to avoid pregnancy during treatment with Dosil. Oral contraceptives (hormonal) may not be effective, as taking Dosil reduces their contraceptive effect, and it is recommended to use barrier methods.
Breastfeeding
The use of Dosil during breastfeeding is not recommended, as it may cause bone and tooth development disorders in the infant.
Driving and operating machinery
There is no evidence that Dosil affects the ability to drive or operate machinery.
This medication contains lactose and wheat starch
This medication contains lactose. If your doctor has indicated that you have a certain sugar intolerance, consult with them before taking this medication.
This medication contains wheat starch, equivalent to 100 ppm of gluten, which should be taken into account by patients with celiac disease.
Patients with wheat allergy (other than celiac disease) should not take this medication.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Remember to take your medication. It is essential to take the capsules regularly at the same time of day.
Your doctor will indicate the duration of treatment with this medication. Do not discontinue treatment until your doctor tells you to, even if you have started to improve.
The dose will be established by the doctor based on your individual characteristics and the type of infection. As a general rule,the usual dose and frequency of administration is as follows:
Adults:
- The usual dose is 200 mg of doxycycline (2 capsules of 100 mg) on the first day of treatment, administered in a single dose or divided into two doses, and then continue with 100 mg of doxycycline (1 capsule) to complete the treatment, administered in a single dose or divided into two doses.
- For the treatment of more severe infections (particularly chronic urinary tract infections), 200 mg should be administered daily throughout the treatment period. In general, treatment should continue for at least 24 to 48 hours after the disappearance of symptoms and fever.
Specific dosing guidelines for adults:
Indication | Dosing guideline | Treatment duration |
Uncomplicated nongonococcal urethritis, cervicitis, and proctitis | 100 mg every 12 hours. An antimicrobial agent with adequate spectrum should be administered, preferably in a single dose. | For at least 7 days. |
Granuloma inguinal (donovanosis) | 100 mg every 12 hours. | For at least 21 days |
Pelvic inflammatory disease | Outpatients:100 mg of doxycycline every 12 hours, along with an intramuscular cefalosporin or other third-generation cefalosporin administered parenterally, and probenecid 1g administered orally in a single dose. | For 14 days. |
Syphilis in patients allergic to penicillin, except pregnant women | 100 mg of doxycycline every 12 hours. | For 2 weeks. In the case of late and latent syphilis, if it is known that the duration of the infection has been more than 1 year, the treatment duration should be 4 weeks. |
Acute epididymitis | 100 mg every 12 hours, along with a cefalosporin with adequate spectrum in a single dose. | For 10 days. |
Brucellosis | 100 mg of doxycycline every 12 hours. | For 6 weeks. Along with streptomycin administered intramuscularly for 2-3 weeks. |
Cholera | 300 mg of doxycycline. | Single dose. |
Lyme disease (early stages 1 and 2) | 100 mg of doxycycline orally every 12 hours. | For 10-60 days, depending on clinical signs and symptoms and response. |
Recurring fevers transmitted by lice and ticks | 100 mg or 200 mg, depending on severity, or, | Single dose. |
Alternatively, for tick-borne fever, 100 mg of doxycycline every 12 hours may be administered. | For 7 days as an alternative to reduce the risk of persistence or recurrence of tick-borne fever. | |
Treatment of chloroquine-resistant malaria | 200 mg of doxycycline daily(1) | For at least 7 days. |
Treatment of cutaneous, intestinal, or pulmonary carbuncle | 100 mg of doxycycline every 12 hours initially administered intravenously and then continued orally as soon as appropriate. | Treatment duration should be 60 days, except in the case of cutaneous carbuncle without systemic involvement (not reaching the bloodstream), in which case treatment duration may be reduced to 7-10 days. |
Severe acne vulgaris | 50-100 mg of doxycycline daily. | For 12 weeks. |
Malaria prevention | 100 mg of doxycycline daily. | Prevention should start 1-2 days before traveling to endemic areas. Continue this dosing regimen during travel to endemic areas and for 4 weeks after leaving the endemic area. |
Prevention of anthrax after exposure to bacteria causing this disease | 100 mg of doxycycline every 12 hours. | For 60 days. |
(1)Due to the potential severity of the infection, a rapid-acting antimalarial agent such as quinine should always be administered in combination with doxycycline. Quinine dosing recommendations vary by geographic area.
There are different doses available for various dosing regimens.
Patients with liver dysfunction
Doxycycline should be administered with caution in patients with liver dysfunction.
Patients with renal insufficiency
Doxycycline does not require dose adjustment in patients with renal dysfunction.
Patients of advanced age
No dose adjustment is necessary.
Use in children and adolescents
In children under 8 years, the use of Dosil is not recommended.
In children over 8 years and up to 45 kg, there is another presentation more suitable for dose adjustment.
In children over 8 years and over 45 kg, the same dose as in adults is recommended.
Administration form
Oral administration.
This medication should be taken during a meal, accompanied by a large glass of water or milk.
It is essential to wait at least 1 hour after taking the medication before lying down or going to bed.
The above recommendations aim to prevent the occurrence of digestive problems, especially esophageal ulcers.
If you take more Dosil than you should
Information for healthcare professionals: In case of overdose, discontinue administration, initiate symptomatic treatment, and supportive measures.
Peritoneal dialysis does not alter plasma elimination half-life and therefore would not be beneficial in treating overdose.
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 Dosil
If you forget to take a dose, take the next one at the usual time. Do not take a double dose to compensate for the missed doses. It is essential to take the medication regularly at the same time of day.
Like all medications, this medication may cause side effects, although not everyone will experience them.
The following side effects have been observed in patients who have taken tetracyclines, including doxycycline, listed in order of their frequency of occurrence:
Frequent side effects (may affect up to 1 in 10 people):
Allergic reactions (including skin and mucous membrane edema (angioedema), exacerbation of lupus erythematosus, pericarditis, hypersensitivity, serum disease, Henoch-Schonlein purpura, hypotension, shortness of breath (dyspnea), tachycardia (rapid pulse), peripheral edema, and red, elevated, itchy skin lesions (urticaria), headache, nausea, vomiting, exaggerated skin reaction to sunlight or ultraviolet radiation, skin rash (including erythematous and maculopapular types).
Rare side effects (may affect up to 1 in 100 people):
Digestive alterations (gastritis).
Infrequent side effects (may affect up to 1 in 1,000 people):
Severe destruction of red blood cells (hemolytic anemia), decreased platelet count (thrombocytopenia), alteration in white blood cell count: decreased neutrophil count (neutropenia) or increased eosinophil count (eosinophilia), drug-induced rash with eosinophilia or systemic symptoms, brown-black microscopical discoloration of the thyroid gland, decreased appetite, increased intracranial pressure (benign intracranial hypertension) in adults, fontanelle bulging (unossified skull space in young children) in children, tinnitus, facial redness (rubefaction), altered stool volume or consistency (diarrhea, pseudomembranous colitis), esophageal ulcers, esophagitis, enteritis, anogenital inflammatory lesions, dysphagia, abdominal pain, glossitis, liver dysfunction, hepatitis, and liver damage, toxic epidermal necrolysis, severe skin and mucous membrane inflammation (Stevens-Johnson syndrome), multiform erythema, extensive skin peeling (dermatitis exfoliativa), nail loss (photoonycholysis), arthralgia, and myalgia, elevated blood urea.
Side effects of unknown frequency (cannot be estimated from available data):
Jarisch-Herxheimer reaction, which is characterized by fever, chills, headache, muscle pain, and skin rash, and usually resolves spontaneously. It occurs shortly after the start of doxycycline treatment for spirochetal infections, such as Lyme disease.
Like all tetracyclines, doxycycline may cause permanent discoloration of teeth (from grayish-brown to yellowish) and alteration of bone growth.
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Store in the original packaging to protect it from moisture.Do not store at a temperature above 30°C.
Do not usethis medicationafter the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through drains or in the trash. Dispose of packaging and unused medications at the SIGRE collection pointat the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and unused medications. By doing so, you will help protect the environment.
Composition of Dosil
- The active ingredient is doxycycline. Each capsule contains 100 mg of doxycycline (as hyclate).
- The other components are:
Content of the capsule:calcium hydrogen phosphate, magnesium trisilicate, wheat starch, lactose monohydrate, and magnesium stearate.
Appearance of the product and content of the packaging
Dosil is presented in the form of hard green capsules.
Aluminum and PVC blister.
Each package contains 14 or 500 hard capsules.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Laboratorios Llorens, S.L.
Ciudad de Balaguer, 7-11
08022 Barcelona
Responsible for manufacturing
Laboratorios Llorens S.L.
C/ Llacuna, 19-21
08005 Barcelona
Last review date of this leaflet: 04/2024
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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