Loperamide Hydrochloride
This Medication Should Always be Taken Exactly as Described in the Patient Leaflet or as Advised by a Doctor or Pharmacist.
The Active Substance of Loperamid APTEO MED is Loperamide Hydrochloride, a Substance with Anti-Diarrheal Action. The Medication Prolongs the Time of Passage of Food Through the Intestines, Reduces Water and Electrolyte Excretion, and Reduces the Immediate Need for Defecation.
Loperamid APTEO MED is Used:
If After 2 Days There is no Improvement or the Patient Feels Worse, They Should Consult their Doctor.
Before Starting Treatment with Loperamid APTEO MED, the Patient Should Discuss it with their Doctor or Pharmacist.
Treatment of Diarrhea with Loperamid APTEO MED is Only Symptomatic.
In Every Case Where it is Possible to Determine the Cause of Diarrhea, When Justified (or Indicated), the Doctor will Prescribe Appropriate Treatment.
In Patients with Diarrhea, Especially in Young People, the Elderly, and Weakened Patients, Dehydration and Excessive Electrolyte Loss may Occur. Therefore, During Diarrhea, it is Necessary to Take More Fluids than Usual to Compensate for these Deficiencies.
If After Administration of the Medication in Acute Diarrhea, Symptoms do not Subside Within 48 Hours, the Patient Should Discontinue the Use of Loperamid APTEO MED and Consult their Doctor.
Patients with AIDS Taking Loperamid APTEO MED for Diarrhea Should Immediately Discontinue the Medication and Consult their Doctor if they Experience any Early Symptoms of Abdominal Distension. In Patients with AIDS and Infectious Colitis Caused by Both Viruses and Bacteria, Isolated Cases of Toxic Megacolon have been Reported During the Use of Loperamide.
In Patients with Liver Function Disorders, the Product Loperamid APTEO MED Should be Used with Caution Due to Reduced Metabolism Associated with the First-Pass Effect in the Liver. In these Patients, Relative Overdose of the Medication may Occur, Leading to Toxic Effects on the Central Nervous System.
This Medication Should not be Taken for a Purpose Other than its Indicated Use (See Section 1) or in Higher Doses than Recommended (See Section 3). In Patients Taking Too High Doses of Loperamide (the Active Substance of Loperamid APTEO MED), Serious Heart Rhythm Disorders (Including Accelerated or Irregular Heart Rhythm) have been Noted.
Patients with Diagnosed Irritable Bowel Syndrome (IBS) Should Discuss Treatment with their Doctor or Pharmacist Before Taking the Medication, Especially if:
Loperamid APTEO MED Should not be Used in Children Under 6 Years of Age or in Patients with Irritable Bowel Syndrome Under 18 Years of Age.
The Patient Should Inform their Doctor or Pharmacist About all Medications They are Currently Taking or Have Recently Taken, as Well as any Medications They Plan to Take.
It is Especially Important to Inform the Doctor or Pharmacist About the Use of:
See Section 3.
If the Patient is Pregnant or Breastfeeding, Thinks They May be Pregnant, or is Planning to Have a Child, They Should Consult their Doctor or Pharmacist Before Taking this Medication.
Small Amounts of Loperamide may Pass into Breast Milk, Therefore, it is not Recommended to Use the Medication During Breastfeeding.
Pregnant or Breastfeeding Patients Should Consult their Doctor to Determine the Appropriate Treatment.
The Effect of the Medication on Fertility has not been Studied.
During the Treatment of Diarrhea with Loperamide, the Following Symptoms may Occur: Reduced Awareness, Fatigue, Dizziness, or Drowsiness, Therefore, Caution Should be Exercised When Driving or Operating Machines.
If the Patient has Previously been Diagnosed with Intolerance to Some Sugars, They Should Consult their Doctor Before Taking the Medication.
Loperamid APTEO MED Should be Taken Exactly as Described in the Patient Leaflet or as Advised by a Doctor. In Case of Doubt, the Patient Should Consult their Doctor or Pharmacist.
Loperamid APTEO MED Should be Taken Orally, with a Drink of Fluid.
Diarrhea may Subside After a Single Dose. In this Case, the Medication Should not be Continued. During Diarrhea, it is Necessary to Drink More Fluids than Usual. This is Especially Important in the Case of Young People, the Elderly, and Weakened Patients.
Acute and Chronic Diarrhea:
Adults, Children, and Adolescents Over 6 Years of Age
Acute Diarrhea: Initially, the Dose is 2 Capsules (4 mg) for Adults and 1 Capsule (2 mg) for Children, and then 1 Capsule (2 mg) After Each Loose Stool.
Chronic Diarrhea: the Initial Dose is 2 Capsules (4 mg) per Day for Adults and 1 Capsule (2 mg) per Day for Children. This Initial Dose Should be Modified Until 1 to 2 Normal Stools per Day are Achieved, Which is Usually Achieved by Taking a Maintenance Dose of 1 to 6 Capsules (2 mg to 12 mg) per Day.
Maximum Daily Dose in Acute and Chronic Diarrhea: 8 Capsules (16 mg) per Day for Adults and Children; in Children, the Dose Must be Adjusted According to Body Weight (3 Capsules/20 kg Body Weight). The Dose Should not Exceed the Maximum Recommended Dose.
If in the Treatment of Acute Diarrhea, Symptoms Worsen or do not Subside Within 48 Hours of Taking Loperamid APTEO MED, the Patient Should Discontinue the Medication and Consult their Doctor.
Symptomatic Treatment of Acute Episodes of Diarrhea Associated with Irritable Bowel Syndrome:
Adults, Persons Over 18 Years of Age
Initially 2 Capsules (4 mg), and then 1 Capsule (2 mg) After Each Loose Stool or as Advised by a Doctor. The Maximum Daily Dose Should not Exceed 6 Capsules (12 mg).
In the Case of Repeated Episodes of Diarrhea in Irritable Bowel Syndrome, Loperamid APTEO MED can be Used for up to 2 Weeks, but in Each Episode of Diarrhea Lasting Longer than 48 Hours, the Patient Should Consult their Doctor.
Children
Loperamid APTEO MED Should not be Used in Children Under 6 Years of Age, or in Patients with Irritable Bowel Syndrome Under 18 Years of Age.
Using Loperamid APTEO MED in the Elderly
In the Elderly, Dose Adjustment is not Necessary.
Using Loperamid APTEO MED in Patients with Renal Impairment
In Patients with Renal Impairment, Dose Adjustment is not Necessary.
Using Loperamid APTEO MED in Patients with Hepatic Impairment
In Patients with Hepatic Impairment, the Medication Should be Used Under Medical Supervision, as Caution is Advised and Close Monitoring for Signs of Central Nervous System Toxicity is Necessary.
In Case of Taking a Higher Dose of the Medication than Recommended, the Patient Should Immediately Consult their Doctor or Go to the Nearest Hospital.
In Case of Overdose, the Following Symptoms may Occur:
Accelerated Heart Rate, Irregular Heart Rhythm, Changes in Heart Rhythm (These Symptoms may have Severe, Life-Threatening Consequences), Muscle Stiffness, Uncoordinated Movements, Drowsiness, Pupillary Constriction, Urination Difficulties, Shallow Breathing, Slow Breathing. In Children, the Reaction to Taking High Doses of Loperamid APTEO MED is Stronger than in Adults. If a Child Takes Too High a Dose of the Medication or Experiences any of the Above Symptoms, the Parent or Guardian Should Immediately Consult a Doctor.
In Case of Missing a Dose, the Patient Should Take the Next Dose After the Next Loose Stool (Defecation).
The Patient Should not Take a Double Dose to Make up for the Missed Dose.
Like all Medications, this Medication can Cause Adverse Reactions, Although not Everybody gets them.
Rare(May Affect up to 1 in 1000 People):
Uncommon(May Affect Less than 1 in 100 People):
Common(May Affect Less than 1 in 10 People):
If the Patient Experiences any Adverse Reactions, Including any Adverse Reactions not Listed in the Leaflet, They Should Inform their Doctor or Pharmacist. Adverse Reactions can be Reported Directly to the Department for Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products:
Aleje Jerozolimskie 181C, 02-222 Warsaw. Tel.: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Adverse Reactions can also be Reported to the Marketing Authorization Holder.
Reporting Adverse Reactions will Help to Gather More Information on the Safety of the Medication.
Do not Store Above 25°C.
The Medication Should be Stored in a Place that is Inaccessible to Children.
Do not Use this Medication After the Expiry Date Stated on the Packaging. The Expiry Date Refers to the Last Day of the Specified Month.
Medications Should not be Disposed of via Wastewater or Household Waste. The Patient Should Ask their Pharmacist how to Dispose of Medications that are no Longer Needed. This will Help Protect the Environment.
The Active Substance of the Medication is Loperamide Hydrochloride. Each Capsule Contains 2 mg of Loperamide Hydrochloride.
The Other Ingredients are:
Corn Starch (Dried), Lactose (DCL 21), Polysorbate 80, Talc, Colloidal Silica (Anhydrous), Magnesium Stearate. Capsule Shell: Body: Gelatin, Purified Water, Sodium Lauryl Sulfate, Erythrosine (E 127), Iron Oxide (E 172), Titanium Dioxide (E 171), Cap: Gelatin, Purified Water, Sodium Lauryl Sulfate, Iron Oxide Yellow (E 172), Indigo Carmine (E 132), Titanium Dioxide (E 171); Ink: Shellac, Iron Oxide (E 172), Potassium Hydroxide.
Hard Gelatin Capsule, Grey-Green in Colour, Size "4", with the Imprint "24" on the Body and "C" on the Cap, Filled with a White or Almost White Powder.
Package Size:
8, 10 or 20 Capsules in PVC/Aluminium Blister Packs in a Cardboard Box.
Synoptis Pharma Sp. z o.o.
ul. Krakowiaków 65
02-255 Warsaw
tel. 607 696 231
e-mail: infodn@synoptispharma.pl
Synoptis Industrial Sp. z o.o.
ul. Rabowicka 15
62-020 Swarzędz
Date of Last Update of the Leaflet:August 2024
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.