Ambroxol Hydrochloride Tablets Instructions
Please read the instruction manual carefully and use as directed or under the Purchase and use under the guidance of a pharmacist
[Drug Name]
Generic Name: Ambroxol Hydrochloride Tablets
Trade Name: Ampersol
English name:Ambroxol Hydrochloride Tablets
Hanyu Pinyin:Yansuan Anxiusuo Pian
[Cheng
Participation
This product contains amiloride hydrochloride per tablet30mg, with the following excipients: lactose, calcium hydrogen phosphate, corn starch, sodium carboxymethyl starch, colloidal silicon dioxide, and magnesium stearate.
[sex
Situation
This product is a white tablet or off-white tablet.
[Category of action]
This product is an over-the-counter drug in the category of expectorants.
[Suitable for
Applicable
Sickness]
For those with thick sputum that cannot be easily coughed up.
[Regulation
Gauge
30mg
[dosage]
Orally. Adults, one time1-2tablets a day3times a day, after meals.
[Adverse Reactions]
Sometimes rash, nausea, stomach upset, 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 Epidermolysis Bullosa(TEN)and Acute generalized eruptive pustulosis.
If serious adverse reactions occur, discontinue treatment immediately.
[PROHIBITED
Absence
Not recommended for those with known hypersensitivity to Ambroxol Hydrochloride or other ingredients of this product.
Pregnancy Head3months of pregnancy is contraindicated.
[Caution][Caution “font-family:Times New Roman”>
1.This product is not recommended for pregnant and lactating women and may be used with caution if necessary; it is contraindicated in women during the first3 months 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 and sputum symptoms, and attention should be paid to the cause of coughing and sputum when using7after 7days without improvement, seek prompt medical attention.
5.If overdose or serious adverse reactions occur, seek immediate medical attention.
6.Such as allergy to this product is prohibited, allergic persons should use with caution.
7.The use of this product is prohibited when its properties are changed.
8.Please keep this product out of the reach of children.
9.Must be used by children 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 epidermolysis bullosa, with expectorants(such as amiloride hydrochloride =”font-family:Times New Roman”>)duration of medication 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 influenza-like prodromal symptoms such as fever, body aches, rhinitis, cough and sore throat. These nonspecific influenza-like prodromal symptoms can be misleading, and symptomatic treatment with cough and cold medications may be initiated. 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 contains102mg of lactose per tablet, maximum recommended daily dose(180mg )contains612mg Lactose. With rare hereditary galactose intolerance, Lapplactase deficiency or glucose =”font-family:Times New Roman”>-galactose malabsorption should not be taken by patients.
14.This product has no effect on the ability to drive and operate machinery.
[Drug Interactions]
1.Concurrent administration of this product with antibiotics (amoxicillin, cefuroxime, erythromycin, doxycycline) may result in elevated antibiotic concentrations in lung tissue.
2.If used with If used with other drugs, drug interactions may occur, consult your physician or pharmacist for details.
[Pharmacological Action]
This product is a mucolytic agent that increases the secretion of respiratory mucosal plasma glands and decreases the secretion of mucus glands, thereby reducing the viscosity of sputum. It promotes the secretion of lung surface active substances and increases the movement of bronchial cilia so that sputum can be easily coughed out.
[storage
Storage
Store under shade and seal.
[package
Package
Polyvinyl chloride solid pharmaceutical hard tablets/pharmaceutical aluminum foil, (1))10pieces×1plate; (2)10tablets×2board; (2)10pieces×4 board.
[with
Effective
Duration
60months
[Executive Standard]
[Approval number]
State Drug CertificateH19990228
[Date of revision of instruction]
[Drug Marketing Authorization Holder]
Name Name: Sandoz (China) Pharmaceuticals Ltd
Registered Address: Huiling Road, National Health Base, Torch Development Zone, Zhongshan, Guangdong8No.
Postal Code: 528437
Phone Number: 0760-85319341
Fax Number:0760-85310695
Net =”font-family:equals”>Address:www.sandoz.com.cn
[Manufacturer]
Company name: Sandoz (China) Pharmaceutical Co. family:Arial”>
Manufacturing Address: Huiling Road, National Health Base, Torch Development Zone, Zhongshan, Guangdong8No.
Postal Code:528437
Contact the manufacturer if you have any questions.