Class A
Ambroxol Hydrochloride Tablets Instructions
Please read the instructions carefully and use as directed or buy and use under the guidance of your pharmacist
[Drug Name]
Generic name: Ambroxol Hydrochloride Tablets
Trade Name: Belay®
English Name: Ambroxol Hydrochloride Tablets
Hanyu Pinyin: Yansuan Anxiusuo Pian
[Cheng
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This product contains 30 mg of the main ingredient Ambroxol Hydrochloride per tablet. family:Arial”>, excipients are cellulose- Lactose, pregelatinized starch, silicon dioxide, magnesium stearate.
[sex
Situation
This product is a white or off-white tablet. [Category of action]
This product is an over-the-counter drug in the expectorant category.
[Suitable for
Applicable
Syndromes]
For those with thick sputum that is not easily coughed up.
[gauge
Gauge]
30mg
Orally. Adults, once1 to 2tablets a day3times Take after meals.
[Adverse Reactions]
Sometimes rash, nausea, upset stomach, lack of appetite, abdominal pain, diarrhea.
Other allergic reactions, including anaphylaxis, angioedema, urticaria, and pruritus.
Other gastrointestinal reactions such as gastrointestinal dysfunction including vomiting and dyspepsia.
Other neurological reactions, including headache and dizziness.
Rare severe skin reactions, including erythema multiforme, Stevens-Johnson syndrome(SJS)/Toxic epidermal necrolysis relaxans(TEN)and acute generalized eruptive pustulosis.
If serious adverse reactions occur, discontinue treatment with this product immediately.
[PROHIBITED
Never
Not recommended for those with known hypersensitivity to Ambroxol Hydrochloride or other ingredients of this product.
Pregnancy head33 months.
[Precautions]
1.Pregnant and lactating women This product is not recommended; if necessary, use with caution as directed by a physician and is contraindicated in women during the first3months of pregnancy.
2.Please consult your physician or pharmacist for dosage for children.
3.Concomitant use with central cough suppressants (e.g., dextromethorphan, etc.) should be avoided to avoid blockage of the airway by diluted sputum.
4.This product is a mucus regulator and is only useful for coughing up sputum symptoms. When using this product, attention should be paid to the cause of coughing and coughing up sputum, and if there is no improvement after using7days, prompt medical attention should be sought.
5.If overdose or serious adverse reactions occur, seek immediate medical attention.
6.Discontinued for allergic individuals. Use with caution for allergic individuals.
7.Forbidden to use when the properties of this product have changed.
8.Please keep this product out of the reach of children.
9.Children must be used under adult supervision.
10.If you are using other drugs, consult your physician or pharmacist before using this product.
11.A few cases of severe skin damage have been reported, such as Stevens-Johnson syndrome and toxic epidermal necrolysis loosening syndrome, with expectorants(such as amiloride hydrochloride) =”font-family:isoline”>drug duration is relevant. Most of these cases can be explained by the severity of the patient’s underlying disease and/ or combined medications. In addition, in the early stages of Stevens-Johnson syndrome or toxic epidermolysis bullosa, patients may first present with nonspecific flu-like prodromal symptoms such as fever, body aches, rhinitis, cough, and sore throat. These non-specific flu-like prodromal symptoms can be misleading and may start with symptomatic treatment with cough and cold medications. Therefore, if new skin or mucosal lesions develop, seek immediate medical attention and, as a precautionary measure, discontinue the use of amiloride hydrochloride.
12.For patients with impaired renal function, this product should be used only after consultation with a physician.
13.This product contains154mg of cellulose per tablet-lactose, equivalent to a maximum recommended daily dose of 115.5mg lactose (120mg)contains462mg of lactose. With rare hereditary galactose intolerance,Lapplactase deficiency or glucose-galactose malabsorption should not be taken by patients with lactase deficiency or glucosegalactose malabsorption. –
14.This product has no effect on the ability to drive or operate machinery.
[Drug Interactions]
1. Concurrent administration of this product with antibiotics (amoxicillin, cefuroxime, erythromycin, doxycycline) may result in increased antibiotic concentrations in lung tissue.
2. Drug interactions may occur if used concurrently with other drugs; consult your physician or pharmacist for details.
[Pharmacological effects]
This product is a mucolytic agent that increases the secretion of respiratory mucosal plasma glands and decreases the secretion of mucus glands, thereby reducing sputum viscosity, promoting the secretion of lung surface active substances, and increasing Bronchial cilia movement, so that sputum can be easily coughed out.
[storage
Hiding
Store under 30°C under shade, sealed.
[package
Package
Polyvinyl chloride solid pharmaceutical hard tablets and aluminum foil for pharmaceutical packaging, 2 plates per box, 10 tablets per plate.
[with
effective
Period】
18 months
[Executive Standard]
/
[approval number]
GuoYaoZhenZhiH19980016
[Date of revision of instruction]
[Manufacturer]
Company name: Jiangsu Hengrui Pharmaceutical Co. :Arial”>
Production Address: Lianyungang Economic and Technological Development Zone, Huanghe Road No. 38
Postal Code:222047
Phone Number: 800-8283900 400-8283900
Fax Number: 0518-85463261
Website: http://www.hrs.com.cn
If you have any questions, please contact the manufacturer