Medication info

Daewon Atropine Sulfate Injection

Prescription medicationIntramuscular injection · Intravenous injection · Subcutaneous injection
Ingredient · strength
Atropine Sulfate Hydrate›0.5mg / 1mL
Manufacturer / importer
Daewon Pharmaceutical Co., Ltd.
Appearance
A colorless and transparent liquid is filled in a brown ampoule, which has an unpleasant irritating bitter taste. For export: A colorless and transparent liquid is filled in an ampoule, which has an unpleasant irritating bitter taste.
Packaging
Domestic use: 1mL/ampoule x 50, export: 1mL/ampoule x 10, 50
Approval status
Active

MFDS item code 196400054 · Notified 1964.03.03 · Insurance code 671801141

Summary

Main use
Relief of spasms and excessive secretions; treatment of bradycardia and conduction disorders; preanesthetic medication and treatment of poisoning
Who receives it
Adults
Adult administration
○ Adults 1. Inject 0.5 mg of atropine sulfate hydrate subcutaneously or intramuscularly per dose. Intravenous injection may be used depending on the circumstances. 2. Organophosphate insecticide poisoning 1) Mild: Inject 0.5-1 mg of atropine sulfate hydrate subcutaneously. 2) Moderate: Inject 1-2 mg of this medicine subcutaneously or intramuscularly and repeat at 20-30-minute intervals if needed. 3) Severe: Inject 2-4 mg of this medicine intravenously and repeat according to symptoms until signs of atropine saturation appear. Adjust the dose as appropriate according to age and symptoms.

Ingredients

Manufacturer
Daewon Pharmaceutical Co., Ltd.

Efficacy & effects

Relief of spasms and excessive secretions; treatment of bradycardia and conduction disorders; preanesthetic medication and treatment of poisoning

  • Spasmodic abdominal pain
  • biliary and ureteral colic
  • spastic constipation
  • atrioventricular conduction disorders
  • vagally-mediated bradycardia
  • poisoning by organophosphate insecticides and parasympathetic stimulants
View approved original text

This medication is used to relieve spasmodic pain in the gastrointestinal tract as well as acute pain in the bile ducts and ureters. It also improves spastic constipation and regulates excessive secretions and motility caused by gastric and duodenal ulcers. It is effective for atrioventricular conduction disorders and vagally-mediated bradycardia, and is also utilized for pre-anesthetic medication. Additionally, it is used to treat poisoning caused by organophosphate insecticides or parasympathetic stimulants. Overall, this medication acts effectively on various gastrointestinal and cardiac-related disorders and intoxications.

How it is given

Adult administration

○ Adults 1. Inject 0.5 mg of atropine sulfate hydrate subcutaneously or intramuscularly per dose. Intravenous injection may be used depending on the circumstances. 2. Organophosphate insecticide poisoning 1) Mild: Inject 0.5-1 mg of atropine sulfate hydrate subcutaneously. 2) Moderate: Inject 1-2 mg of this medicine subcutaneously or intramuscularly and repeat at 20-30-minute intervals if needed. 3) Severe: Inject 2-4 mg of this medicine intravenously and repeat according to symptoms until signs of atropine saturation appear. Adjust the dose as appropriate according to age and symptoms.

Precautions

This medication is an injectable ampoule, and care should be taken when cutting the container as glass fragments may be mixed in. Special caution should be taken when being administered to children or the elderly. This medication should not be used in patients with glaucoma, urinary disorders due to prostatic hypertrophy, patients with paralytic ileus, those allergic to this medication, and patients with asthma. It should be administered cautiously to patients with prostatic hypertrophy, severe cardiac disease, ulcerative colitis, hyperthyroidism, individuals in high-temperature environments, and patients over 40 years old. When using this medication, pupils may dilate, and symptoms such as inability to accommodate, glaucoma, and blurred vision may appear. Additionally, neurological symptoms such as headaches and dizziness, as well as gastrointestinal symptoms like dry mouth, nausea, and constipation may occur. There may also be rapid heartbeat or difficulty in breathing, and if skin rashes or allergic symptoms appear, use should be discontinued immediately. If severe allergic reactions occur, appropriate treatment is necessary. Urinary disturbances may occur, and facial flushing may also be experienced. During the use of this medication, visual disturbances might occur, so it is advisable to avoid driving vehicles or operating dangerous machinery. When using with other medications, be cautious of interactions. Using with anticholinergic drugs or certain antidepressants, antihistamines, cardiac glycosides, etc., may enhance effects or worsen side effects. It is advisable for women who are pregnant or of childbearing potential, as well as nursing mothers, to avoid using this medication as it may affect the fetus or newborn, potentially causing increased heart rate, and could reduce milk secretion. Safety in children has not been established, and there is a lack of experience with its use. Elderly individuals should use this medication with more caution since side effects such as glaucoma, memory impairment, dry mouth, urinary difficulties, and constipation may more easily occur.

Side effects

  • pupil dilation
  • accommodation disorder
  • glaucoma
  • blurred vision
  • headache
  • heaviness
  • visual disturbances
  • dizziness
  • dry mouth
  • nausea
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  • vomiting
  • difficulty swallowing
  • constipation
  • palpitations
  • respiratory disorders
  • rash
  • shock
  • anaphylactic symptoms
  • tachycardia
  • systemic flushing
  • sweating
  • facial swelling
  • urination disorders
  • facial flushing

Not everyone experiences these, and they can vary from person to person.

Storage

This medication may be sensitive to light, therefore, it should be stored in a light-protective container that does not allow light to enter. It is also important to store it in a sealed container to avoid contact with air.

Appearance and packaging

Appearance

A colorless and transparent liquid is filled in a brown ampoule, which has an unpleasant irritating bitter taste. For export: A colorless and transparent liquid is filled in an ampoule, which has an unpleasant irritating bitter taste.

Package unit

Domestic use: 1mL/ampoule x 50, export: 1mL/ampoule x 10, 50

Same-ingredient medicines

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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.