Medication info

Nafnil Tablets (Nafronil Oxisalate)

Prescription medicationExpired
Ingredient · strength
Nafronyl Oxalate›Strength being verified
Manufacturer / importer
Bivicon Pharmaceutical Co., Ltd.
Appearance
White round film-coated tablets
Packaging
30 tablets/bottle, 90 tablets/bottle
Approval status
Expired

MFDS item code 201308295 · Notified 2013.07.19

This product's status changed to Expired on 2023.07.19. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of peripheral vascular disorders
Who uses it
Adults
Adult dosage
Administer 100 mg of nafronyl oxalate orally 3 times daily.

Ingredients

Manufacturer
Bivicon Pharmaceutical Co., Ltd.

Efficacy & effects

Improvement of peripheral vascular disorders

  • Peripheral vascular disorders
View approved original text

Peripheral vascular disorders occur when blood circulation in peripheral areas such as hands and feet is not smooth, leading to various symptoms. This medication is used for improving blood circulation and alleviating symptoms caused by peripheral vascular disorders.

Dosage and Administration

Adult dosage

Administer 100 mg of nafronyl oxalate orally 3 times daily.

Precautions

This medication should not be used in patients with acute myocardial infarction or early-stage hemorrhagic injuries. Patients with orthostatic control disorders or those who have had allergic reactions to this medication should also avoid it. People with a history of hyperoxaluria or recurrent calcium nephrolithiasis should preferably not take this medication. It should not be administered to patients with myocardial infarction, congestive heart failure, heart conduction defects, severe angina, or severe hypotension. Pregnant women, women who may become pregnant, nursing mothers, patients with poor liver function, or those at risk of seizures should also refrain from using this medication. Special care should be taken when using this medication in patients with impaired renal function or those with coronary artery disease. This medication may cause neurological symptoms such as convulsions, sensory abnormalities, anxiety, drowsiness, insomnia, headache, and dizziness. Gastrointestinal reactions may include loss of appetite, esophagitis, vomiting, gastrointestinal pain, and diarrhea. Allergic reactions such as urticaria or angioedema may also occur, so caution is advised. Liver function abnormalities may lead to hepatitis, jaundice, hepatocyte damage, or liver failure. Impairments in urination or risk of calcium oxalate kidney stones may occur in the kidneys. Cardiovascular issues including hypotension, arrhythmias, angina, syncope, and peripheral edema have also been reported. Blood glucose levels may increase, so diabetic patients should take caution. This medication is not used for hypertension treatment, and adequate fluid intake is important for the prevention of kidney stones. When taking this medication, care should be taken to avoid esophagitis by not consuming it without beverages before sleeping. Combining it with antihypertensives or arrhythmia medications can enhance its effects, so directions from a physician should be followed. It is safer for pregnant or nursing women not to take this medication. In the case of overdose, decreased cardiac function and convulsions may occur, so immediate medical attention should be sought for appropriate treatment. Gastric lavage and activated charcoal administration, cardiovascular function monitoring, the use of a pacemaker, and tranquilizers during convulsions may be required.

Side effects

  • Cerebral spasm
  • sensory disturbances
  • anxiety
  • drowsiness
  • insomnia
  • fatigue
  • headache
  • dizziness
  • loss of appetite
  • esophagitis
Show 21 more
  • vomiting
  • nausea
  • gastric pain
  • diarrhea
  • hives
  • angioedema
  • rash
  • hepatitis
  • cholestasis jaundice
  • acute hepatocellular necrosis
  • increased liver enzymes
  • liver failure
  • urinary disorders
  • calcium oxalate kidney stones
  • hypotension
  • orthostatic regulation disorder
  • arrhythmia
  • angina
  • syncope
  • peripheral edema
  • increased blood glucose

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

Storage

This medication is sensitive to light, so it should be stored in a container that prevents light exposure. Additionally, it is important to maintain a temperature between 1 degree and 30 degrees Celsius while storing the medication to ensure that its components do not change and its efficacy is preserved.

Appearance and packaging

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 90 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

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.