Leaflet: information for the user
Loperamide Hydrochloride 2 mg buccal dispersible tablets
Loperamide hydrochloride
Read this leaflet carefully before you start taking this medicine, as it contains important information for you.
Follow exactly the administration instructions contained in this leaflet or those given by your doctor, or pharmacist.
1. What is Loperamide Hydrochloride and what it is used for
2. What you need to know before starting to take Loperamide Hydrochloride
3. How to take Loperamide Hydrochloride
4. Possible side effects
5. Storage of Loperamide Hydrochloride
6. Contents of the pack and additional information
Salvacolina Flas is an anti-diarrheal that reduces intestinal movements and secretions, resulting in a decrease in liquid stools.
Salvacolina Flas is used for the symptomatic treatment of acute non-specific diarrhea in adults and children over 12 years old.
You should consult a doctor if it worsens or does not improve after 2 days.
Do not take Salvacolina Flas
-If you are allergic to loperamide hydrochloride or any of the other components of this medication (listed in section 6).
-Do not administer to children under 2 years old.
-If there is presence of blood in stool or you have high fever (above 38°C).
-If you have been diagnosed with acute ulcerative colitis (inflammation of the intestine).
-If you suffer from severe diarrhea (pseudomembranous colitis) after taking antibiotics.
-If you suffer from diarrhea caused by an infection caused by organisms such as Salmonella, Shigella or Campylobacter.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Salvacolina Flas.
-If you do not observe improvement in 48 hours or fever, constipation or other symptoms such as abdominal distension or paralytic ileus (absence of intestinal movements) interrupt the treatment and consult your doctor.
-If you suffer from severe diarrhea your body loses more fluids, sugars and salts than normal, so you will need to replenish the fluids by drinking more than usual. Dehydration manifests itself by dry mouth, excessive thirst, decreased urine output, wrinkled skin, dizziness and drowsiness. It is very important to prevent dehydration in children and the elderly.
-Patients with AIDS should discontinue treatment when the first symptoms of abdominal distension appear.
-If you have liver or kidney disease or blood disorders consult your doctor before taking this medication.
-Since the treatment of diarrhea with Salvacolina Flas is only symptomatic, the diarrhea should be treated from its cause, when possible.
Children and adolescents
Do not use in children under 12 years old without consulting a doctor or pharmacist.
Use of Salvacolina Flas with other medications
Inform your doctor or pharmacist if you are taking, have taken recently or may need to take any other medication.
Particularly, inform your doctor or pharmacist if you are taking any of the following medications:
-Ritonavir, saquinavir (used to treat AIDS).
-Quinidine (used to treat heart rhythm disorders).
-Desmopressin (used to treat central diabetes insipidus and nocturnal urinary incontinence in children).
-Itraconazole or ketoconazole (used to treat fungal infections).
-Gemfibrozil (used to reduce cholesterol).
-St. John's Wort (used to improve mood and treat mild depressions).
-Valerian (used to treat mild states of nervousness and anxiety).
-Opioid analgesics (used to treat very intense pain) as they may increase the risk of severe constipation and central nervous system depression (e.g. drowsiness or decreased consciousness).
-Broad-spectrum antibiotics as they may worsen diarrhea caused by antibiotics.
Salvacolina Flas may potentiate the action of similar drugs.
Pregnancy, breastfeeding and fertility
If you are pregnant or breastfeeding, think you may be pregnant or intend to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
The safety of use of this medication during pregnancy has not been established, so pregnant women should not take this medication unless prescribed by a doctor.
Breastfeeding
Women who are breastfeeding should not use this medication without consulting their doctor as small amounts of it may pass into breast milk.
Driving and operating machinery
You may experience drowsiness, dizziness or somnolence during treatment of diarrhea with Salvacolina Flas, so it is recommended not to use hazardous machinery or drive vehicles.
Salvacolina Flas contains aspartame
This medication may be harmful to people with phenylketonuria because it contains aspartame which is a source of phenylalanine.
Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Adults:
2 buccal tablets (4 mg of loperamide hydrochloride) as the initial dose, followed by 1 buccal tablet (2 mg of loperamide hydrochloride) after each diarrheal stool. Do not take more than 8 buccal tablets (16 mg of loperamide hydrochloride) per day.
Children over 12 years:
1 buccal tablet (2 mg of loperamide hydrochloride) after each diarrheal stool. In children, the maximum daily dose should be related to body weight:
Child weight | Maximum number of tablets per day |
From 27 Kg | Maximum 4 tablets |
From 34 Kg | Maximum 5 tablets |
From 40 Kg | Maximum 6 tablets |
From 47 Kg | Maximum 7 tablets |
Patients with liver disease:
They should consult a doctor before taking this medication.
This medication is taken orally.
Place the tablet on the tongue, where it will dissolve quickly and swallow it with saliva.
If you take more Salvacolina Flas than you should
If you have taken too much Salvacolina, contact a doctor or hospital as soon as possible to seek help. Symptoms may include: increased heart rate, irregular heartbeats, heart rhythm disturbances (these symptoms may have potentially serious and life-threatening consequences), muscle stiffness, uncoordinated movements, drowsiness, difficulty urinating, or weak breathing.
Children react more severely to high amounts of Salvacolina than adults. If a child takes an excessive amount or exhibits any of the above symptoms, call a doctor immediately.
In case of overdose or accidental ingestion, go immediately to a medical center or consult the Toxicological Information Service, phone 915 620 420, indicating the medication and the amount ingested.
If you forgot to take Salvacolina Flas
Do not take a double dose to compensate for the missed dose.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication may cause side effects, although not everyone will experience them.
If you experience any of the following side effects, discontinue treatment and consult your doctor: hypersensitivity reactions (redness, itching, or swelling of the skin, difficulty swallowing or breathing), blisters or significant skin peeling, intestinal paralysis (absence of bowel movements or paralytic ileus), abdominal distension, severe abdominal pain, megacolon, and loss or decrease in level of consciousness.
Commonly (may affect up to 1 in 10 patients) may appear:constipation, nausea, gas (flatulence), headache (cephalalgia), and dizziness.
Infrequently (may affect up to 1 in 100 patients) may appear:vomiting, pain or unpleasant sensation in the upper-middle part of the stomach (dyspepsia), dry mouth, abdominal pain or discomfort, drowsiness, and skin discoloration (exanthema).
Rarely (may affect up to 1 in 1000 patients) may appear:intestinal paralysis (absence of bowel movements or paralytic ileus), abdominal distension, megacolon, loss or decrease in level of consciousness, stupor (general unconsciousness), excessive muscle tone (hypertonia), abnormal coordination, skin blisters (bullous eruptions, including Stevens-Johnson syndrome, multiform erythema, and toxic epidermal necrolysis), skin alteration that produces lesions and intense itching (urticaria), itching (pruritus), severe allergic reactions such as swelling of the lips, face, throat, or tongue that may cause difficulty swallowing or breathing (angioedema) including anaphylactic shock, decreased urine output (urinary retention), pupil constriction (miosis), and fatigue.
Unknown frequency (cannot be estimated from available data): Upper abdominal pain, abdominal pain radiating to the back, abdominal tenderness, fever, rapid pulse, nausea, vomiting, which may be symptoms of acute pancreatitis.
Reporting of 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 Medicines for Human Usehttp://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 at a temperature not exceeding 30°C.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at your pharmacy's SIGRE collection point. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Salvacolina Flas
The active ingredient is: loperamide hydrochloride 2 mg per buccal dispersible tablet.
The other components are: mannitol (E-421), magnesium stearate (E-572), microcrystalline cellulose (E-460 I), sodium croscarmellose, aspartame (E-951), anise aroma, apple aroma.
Appearance of the product and content of the packaging
The buccal dispersible tablets are round, white or almost white in color.
Each package of Salvacolina Flas contains 6 or 12 buccal dispersible tablets presented in blister packaging.
Holder of the marketing authorization and responsible for manufacturing
Laboratorios SALVAT, S.A.
Gall, 30-36
08950 Esplugues de Llobregat (Barcelona) Spain
Date of the last review of this leaflet: March 2022
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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