Levocetirizine Dihydrochloride
The Active Substance of Alcetyr is Levocetirizine Dihydrochloride.
Alcetyr is an Antihistamine Medication.
It is Used to Treat Symptoms Associated With:
Before Taking Alcetyr, Discuss with Your Doctor or Pharmacist:
Alcetyr is Not Recommended for Children Under 6 Years of Age, as the Film-Coated Tablets Do Not Allow for Appropriate Dose Adjustment.
Tell Your Doctor or Pharmacist About All Medications You are Currently Taking, or Have Recently Taken, and Any Medications You Plan to Take.
Caution is Advised When Taking Alcetyr with Alcohol or Other Substances that Affect Brain Function.
In Sensitive Patients, Concurrent Use of Cetirizine or Levocetirizine with Alcohol or Other Substances that Affect Brain Function May Cause Additional Decreased Alertness and Reaction Ability.
Alcetyr Can be Taken with or Without Food.
If You are Pregnant, Breastfeeding, or Think You May be Pregnant, or are Planning to Have a Baby, Ask Your Doctor for Advice Before Taking this Medication.
Some Patients Taking Alcetyr May Experience Drowsiness, Fatigue, and Tiredness. Caution is Advised When Driving or Operating Machinery, Until You Know How the Medication Affects You.
However, Special Tests Conducted in Healthy Volunteers After Taking Levocetirizine at the Recommended Dose Did Not Show an Effect on Attention, Reaction Ability, or Driving Ability.
This Medication Contains Lactose. If You Have Been Diagnosed with Intolerance to Some Sugars, You Should Consult Your Doctor Before Taking Alcetyr.
Always Take this Medication Exactly as Your Doctor Has Told You. If You are Not Sure, Ask Your Doctor or Pharmacist.
The Recommended Dose for Adults, Adolescents, and Children Over 6 Years is One Film-Coated Tablet per Day.
The Recommended Dose for Children Aged 6 Years and Above is One Film-Coated Tablet per Day. Alcetyr is Not Recommended for Children Under 6 Years of Age.
In Patients with Renal Impairment, the Dose of Alcetyr May be Reduced Depending on the Severity of the Kidney Disease, and in Children, the Dose Will be Adjusted According to Body Weight; the Dose Will be Determined by the Doctor.
Patient with Severe Renal Insufficiency Should Not Take Alcetyr.
Patient with Hepatic Impairment Should Take the Usual Recommended Dose.
In Patients with Both Hepatic and Renal Impairment, a Lower Dose May be Necessary Depending on the Severity of the Kidney Disease. In Children, the Dose Will be Adjusted According to Body Weight; the Dose Will be Determined by the Doctor.
In Elderly Patients, Dose Adjustment is Not Necessary, Provided Their Renal Function is Normal.
This Medication is for Oral Use Only.
Swallow the Tablets Whole with Water. Alcetyr Can be Taken with or Without Food.
The Duration of Treatment Depends on the Type, Duration, and Severity of the Disease Symptoms and is Determined by the Doctor.
In Case of Overdose, Adults May Experience Drowsiness.
In Children, Initial Excitement and Restlessness, Especially Motor, May Occur, Followed by Drowsiness.
If You Suspect That You Have Taken More Than the Recommended Dose of Alcetyr, Contact Your Doctor, Who Will Decide What Actions Should be Taken.
If You Miss a Dose of Alcetyr, or Take a Lower Dose Than Recommended, Do Not Take a Double Dose to Make Up for the Missed Dose. Take the Next Dose at the Usual Time.
Stopping Treatment with Alcetyr Should Not Have Any Negative Effects. In Rare Cases, After Stopping Treatment, Itching (Intense Itching) May Occur, Even if These Symptoms Did Not Occur Before Starting Treatment. These Symptoms May Resolve on Their Own.
In Some Cases, These Symptoms May be Intense and May Require Resumption of Treatment. These Symptoms Should Resolve After Resuming Treatment.
If You Have Any Further Questions About the Use of this Medication, Ask Your Doctor or Pharmacist.
Like All Medications, Alcetyr Can Cause Side Effects, Although Not Everybody Gets Them.
Common: May Affect Up to 1 in 10 People
Dry Mouth, Headache, Fatigue, and Drowsiness or Drowsiness.
Uncommon: May Affect Up to 1 in 100 People
Feeling of Exhaustion and Abdominal Pain.
Frequency Not Known: Frequency Cannot be Estimated from the Available Data
Other Side Effects, Such as: Palpitations, Rapid Heart Rate, Seizures, Tingling, Dizziness, Fainting, Shaking, Taste Disorders (Taste Disturbances), Feeling of Spinning or Swaying, Vision Disorders, Blurred Vision, Rotatory Eye Movements (Uncontrolled Rotatory Eye Movement), Painful or Difficult Urination, Inability to Completely Empty the Bladder, Edema, Itching (Itching), Rash, Urticaria (Swelling, Redness, and Itching of the Skin), Skin Eruptions, Shortness of Breath, Weight Gain, Muscle Pain, Joint Pain, Aggressive Behavior or Excitement, Hallucinations, Depression, Insomnia, Recurring Suicidal Thoughts or Interest in Suicide, Nightmares, Hepatitis, Liver Function Disorders, Vomiting, Increased Appetite, Nausea, Diarrhea Have Also Been Reported.
Itching (Intense Itching) After Stopping Treatment.
If You Notice the First Symptoms of a Hypersensitivity Reaction, Stop Taking Alcetyr and Seek Medical Attention Immediately. Symptoms of a Hypersensitivity Reaction May Include:
Swelling of the Mouth, Tongue, Face, and (or) Throat, Difficulty Breathing or Swallowing (Chest Tightness or Wheezing) with Urticaria, Sudden Decrease in Blood Pressure Leading to Fainting or Shock, Which Can be Fatal.
If You Experience Any Side Effects, Including Those Not Listed in this Package Leaflet, Tell Your Doctor or Pharmacist. Side Effects Can be Reported Directly to the Department of Adverse Reaction Monitoring of Medicinal Products, Medical Devices, and Biocidal Products:
Jerozolimskie Avenue 181C, 02-222 Warsaw, Tel.: (22) 49 21 301, Fax: (22) 49 21 309,
Website: https://smz.ezdrowie.gov.pl
Side Effects Can Also be Reported to the Marketing Authorization Holder.
By Reporting Side Effects, You Can Help Provide More Information on the Safety of this Medication.
Keep this Medication Out of the Sight and Reach of Children.
Do Not Use this Medication After the Expiration Date Stated on the Carton and Blister After: EXP.
The Expiration Date Refers to the Last Day of the Month.
There are No Special Precautions for Storage.
Medicines Should Not be Disposed of via Wastewater or Household Waste. Ask Your Pharmacist How to Dispose of Medicines No Longer Required. This Will Help Protect the Environment.
White or Almost White, Biconvex, Oval Film-Coated Tablets with a Score Line, with "5" Engraved on One Side and Smooth on the Other Side.
PVC/PVDC/Aluminum Blister Pack, in a Cardboard Box.
The Package Contains 28 Film-Coated Tablets.
Artespharm Sp. z o.o.
Solec Street 81 B, Apt. A-51,
00-382 Warsaw, Poland
Mako Pharma Sp. z o.o.
Wiśniowa Street 9,
05-092 Kiełpin
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