Fexofenadine Hydrochloride
Telfexo Contains Fexofenadine Hydrochloride, Which is an Antihistamine.
Telfexo 120 mg is Indicated for Use in Adults and Children Aged 12 Years and Older to Relieve the Symptoms of Hay Fever (Seasonal Allergic Rhinitis), Such as:
Sneezing, Runny Nose, and Itching of the Nose, Itching, Tearfulness, and Redness of the Eyes.
Telfexo 180 mg is Indicated for Use in Adults and Children Aged 12 Years and Older to Relieve the Symptoms of Chronic Skin Allergic Reactions (Chronic Idiopathic Urticaria), Such as: Itching, Swelling, and Rash.
Before Taking Telfexo, Discuss with the Doctor or Pharmacist if:
If Any of the Above Situations Apply to the Patient or if the Patient Has Any Doubts, Inform the Doctor Before Taking the Medication.
Tell the Doctor or Pharmacist About All Medications the Patient is Currently Taking or Has Recently Taken, as Well as Any Medications the Patient Plans to Take.
If the Patient is Taking Apalutamide (a Medication Used to Treat Prostate Cancer), the Effect of Fexofenadine May be Reduced.
Taking Antacids Containing Aluminum and Magnesium May Affect the Action of Telfexo by Reducing the Amount of Medication Absorbed. Therefore, it is Recommended to Maintain an Interval of Approximately 2 Hours Between Taking Telfexo and Antacids.
If the Patient Takes Fexofenadine with Erythromycin or Ketoconazole, or with a Single Dose of Lopinavir in Combination with Ritonavir, the Concentration of Fexofenadine in the Blood May Increase.
This May Cause an Increase in Side Effects.
If the Patient is Pregnant or Breastfeeding, Thinks She May be Pregnant or is Planning to Have a Child, Consult the Doctor or Pharmacist Before Taking this Medication.
Telfexo Should Not be Used During Pregnancy, Unless it is Absolutely Necessary.
Telfexo is Not Recommended for Use in Breastfeeding Women.
It is Unlikely that Telfexo Will Affect the Ability to Drive or Operate Machinery. However, Before Driving or Operating Machinery, Make Sure that the Medication Does Not Cause Drowsiness or Dizziness.
The Medication Contains Less Than 1 mmol (23 mg) of Sodium per Tablet, Which Means the Medication is Considered "Sodium-Free".
Always Take this Medication Exactly as the Doctor Has Told You. If You are Not Sure, Ask the Doctor or Pharmacist.
Telfexo 120 mg, Film-Coated Tablets:The Usual Dose is One Tablet (120 mg) Once a Day.
Telfexo 180 mg, Film-Coated Tablets:The Usual Dose is One Tablet (180 mg) Once a Day.
Take the Tablets Before a Meal, with a Glass of Water.
If You Take More Telfexo Than You Should, Contact a Doctor or Go to the Nearest Hospital Immediately. Symptoms of Overdose in Adults Include Dizziness, Drowsiness, Fatigue, and Dryness of the Mouth.
Do Not Take a Double Dose to Make Up for a Forgotten Dose.
Take the Next Dose at the Usual Time, as Advised by the Doctor.
If You Plan to Stop Taking Telfexo Before Completing the Treatment, Inform the Doctor. If You Stop Taking Telfexo Earlier Than Recommended, the Symptoms of the Disease May Return.
If You Have Any Further Questions About Taking this Medication, Ask the Doctor or Pharmacist.
Like All Medications, Telfexo Can Cause Side Effects, Although Not Everybody Gets Them.
Common Side Effects(Affecting Less Than 1 in 10 People):
Uncommon Side Effects(Affecting Less Than 1 in 100 People):
Other Side Effects(Frequency Not Known: Cannot be Estimated from the Available Data), Which May Include:
If You Experience Any Side Effects, Including Those Not Listed in this Package Leaflet, Tell the Doctor or Pharmacist. Side Effects Can be Reported Directly to the Department of Medicinal Product Monitoring, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 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 the Medication Out of Sight and Reach of Children.
Do Not Use this Medication After the Expiration Date Stated on the Carton and Blister. The Expiration Date Refers to the Last Day of the Month.
The Entry on the Packaging After the Abbreviation EXP Means the Expiration Date, and After the Abbreviation Lot/LOT Means the Batch Number.
There are No Special Storage Instructions.
Medications Should Not be Disposed of via Wastewater or Household Waste. Ask the Pharmacist How to Dispose of Medications That are No Longer Needed. This Will Help Protect the Environment.
Each Telfexo 120 mg Tablet Contains 120 mg of Fexofenadine Hydrochloride.
Each Telfexo 180 mg Tablet Contains 180 mg of Fexofenadine Hydrochloride.
Telfexo 120 mg Film-Coated Tablets are Peach-Colored, Prolonged-Shape Tablets, Smooth on Both Sides.
Telfexo 180 mg Film-Coated Tablets are Yellow, Prolonged-Shape Tablets, Smooth on One Side, with a Score Line in the Middle of the Other Side.
Telfexo is Packaged in Blisters of 20 Tablets.
Polpharma S.A., ul. Pelplińska 19, 83-200 Starogard Gdański, Poland, tel. +48 22 364 61 01
Polpharma S.A., ul. Pelplińska 19, 83-200 Starogard Gdański, Poland, Chanelle Medical Unlimited Company, Loughrea, Co. Galway, Ireland
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