Itextploroglucinol Tablet (Ploroglucinol Hydrate)
Phloroglucinol Hydrate 80mg
Sublingual Tablet · Prescription medication
Teragen Itext Co., Ltd.
MFDS item code 202201014 · Approved 2022.03.08
Relief of gastrointestinal and biliary tract pain, urinary tract spasmodic pain, and gynecologic pain (spasmodic pain and uterine contractions during pregnancy)
This medication is effective for spasms in the urinary tract, nephritic colic, pain due to dysfunction of the digestive tract and biliary system, and gynecological spasmodic pain. It is also used as an adjunctive treatment for uterine contractions during pregnancy. Overall, it helps alleviate various spasm and pain symptoms.
Adults: Dissolve 160㎎ of phloroglucinol per dose in a glass of water or place it under the tongue, and administer orally when symptoms occur. Adjust the dose appropriately according to age and symptoms.
Children: Dissolve 80㎎ per dose in a glass of water and administer twice daily.
This medication contains the artificial sweetener aspartame, which breaks down into phenylalanine in the body. Therefore, patients with phenylketonuria, a genetic disorder that requires the restriction of phenylalanine, should not take this medication. The maximum allowable daily intake of aspartame should be limited to below 40mg/kg according to WHO guidelines, and for a 60kg adult, care should be taken not to exceed a maximum of 2.4g per day. This medication also contains lactose, so patients with galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption should not take it. Rarely, gastrointestinal symptoms such as nausea or dry mouth may occur during use, and skin allergic reactions or acute generalized pustular psoriasis may also manifest. Additionally, rarely, feelings of malaise or diplopia may occur, so if these symptoms arise, measures such as reducing or temporarily discontinuing the medication should be taken. Since this medication has a muscle relaxant effect, it is advisable to avoid taking it together with analgesics such as morphine or its derivatives. It is preferable for pregnant women, especially in the first trimester, not to take this medication, and it is also advisable not to use it during breastfeeding.
nausea, dry mouth, allergic reactions, acute generalized exanthematous pustulosis, malaise, diplopia
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to light, so it should be stored in a dark place that does not allow light in. Additionally, it should be stored in a tightly sealed container to maintain its effectiveness for a long time by preventing contact with air.
White to pale yellow round sublingual tablet
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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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For anything that needs medical judgment, consult a doctor or pharmacist.
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.