Similasan Hay Fever No. 1 Tabl 80 pcs
Similasan Heuschnupfen Nr. 1 Tabletten 80 Stück
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In stock 14 pcsAnalogues of the product based on the Anatomical Therapeutic Chemical (ATC) Classification - R01Z
Description - Similasan Hay Fever No. 1 Tabl 80 pcs
When is SIMILASAN hay fever No. 1 used?
According to the homeopathic drug picture, SIMILASAN hay fever No. 1 can be used for:? Acute and chronic allergic nasal discomfort? Vasomotor (=nervous) nasal discomfort? Hay fever with burning eyes, tears, swelling of the nasal and ocular canals membranes, itching in the nose, feeling of pressure in the forehead? Dry or dripping hay fever
What should you watch out for?
? This medicine contains 0.24 g of usable carbohydrates per single dose.? If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether SIMILASAN Heuschnu 1 may be taken at the same time.
When should SIMILASAN hay fever No. 1 not be taken or only with caution?
? To date, no application restrictions are known. If used as intended, no special precautionary measures are necessary.? Inform your doctor, pharmacist or druggist if you- suffer from other diseases,- have allergies or- take other medicines (including those you bought yourself) or use them externally!
How do you use SIMILASAN Hay Fever No. 1?
Unless otherwise prescribed by the doctor:Children and adults:? Acute symptoms: 1 tablet several times a day (up to every quarter of an hour). Less frequently as the symptoms improve.? For healing: 1 tablet 3 times a day.Instructions for taking:? Let the tablet dissolve in the mouth (chew it if necessary) and spread it over the surrounding mucous membranes with your tongue.? Can also be taken on an empty stomach.The duration of the effect of a drug administration can vary from person to person. Basically, the intake of the preparation is repeated when the effect wears off or when the symptoms return.
If the drug alleviates acute symptoms, treatment during the entire pollen season (even during a temporarily symptom-free period) is indicated. Under the same condition, it is also advisable to take this medication as a preventive measure (starting approx. 2 months before the expected allergic reaction). Adhere to the dosage given in the package leaflet or prescribed by the doctor.If the desired improvement does not occur when treating a small child/child, they should consult a doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.
What side effects can SIMILASAN Hay fever No. 1 have?
No side effects have been observed for SIMILASAN Hay fever No.1 when used as directed. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. When taking homeopathic medicines, the symptoms can temporarily worsen (initial aggravation).Measures when the symptoms initially worsen:1. Stop taking the preparation until the reaction has subsided.2. Take 1 tablet once. Wait for effect.3. If the reaction is repeated, the same behavior as described under 1. and 2.4. If you no longer feel a reaction, follow the recommendations under "How do you use ...".If the symptoms continue to get worse, discontinue SIMILASAN Hay Fever No.1 and inform your doctor, pharmacist or druggist or your doctortin, pharmacist or druggist.
What else needs to be observed?
? Keep out of the reach of children.? The medicinal product may only be used up to the end of the period marked on the container with
? Store at room temperature (15 - 25 °C).
Your doctor, pharmacist or druggist can provide you with further information.
What does SIMILASAN Hay Fever No. 1 contain?
1 tablet contains: Cardiospermum halicacabum D4 / Luffa operculata D6 / Equal parts Sabadilla (Schoenocaulon officinale) D4 / Thryallis glauca D4 6.25 mg. Excipients: lactose, corn starch and magnesium stearate.
Authorization number
46149 (Swissmedic)
Where can you get SIMILASAN Hay Fever No. 1? Which packs are available?
In pharmacies and drugstores, without a doctor's prescription.
Pack size: 80 tablets
Authorization holder
Similasan AG, CH-8916 Jonen
This leaflet was last checked by the drug authority (Swissmedic) in March 2008.



















