Medication info
Prosetil Tablets (Cefpodoxime Proxetil)

Prosetil Tablets (Cefpodoxime Proxetil)

Prescription medicationTabletOral
Ingredient · strength
Cefpodoxime Proxetil›100mg / 1 tablet
Manufacturer / importer
Geonil Biopharm Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle, 200 tablets/bottle
Approval status
Active

MFDS item code 201800070 · Approved 2018.01.05 · Insurance code 073000100

Summary

Main use
Treatment of respiratory, otorhinolaryngological, skin, breast, genitourinary, and dental infections
Who takes it
Adults · Children
Adult dose
○ Adults: The usual oral dose is 100mg (potency) of cefpodoxime per dose, twice daily after meals. For severe cases or when the response is considered insufficient, the usual oral dose is 200mg (potency) per dose, twice daily after meals. The dose may be adjusted as appropriate according to age, symptoms, etc.
Child dose
○ Infants and children: Administer orally after reconstituting before use. The usual dose is 3mg (potency) of cefpodoxime per Kg of body weight per dose, 2~3 times daily. ○ Infants and children: For severe cases or cases in which the response is considered insufficient, administer 4.5mg (potency) per Kg of body weight per dose orally, 3 times daily. The dose may be adjusted as appropriate according to age, symptoms, etc.

Ingredients

Manufacturer
Geonil Biopharm Co., Ltd.

Efficacy & effects

Treatment of respiratory, otorhinolaryngological, skin, breast, genitourinary, and dental infections

  • Folliculitis
  • pustular acne
  • furuncles
  • carbuncles
  • abscesses
  • shingles
  • cellulitis
  • lymphangitis
  • hand infections
  • purulent paronychia
  • subcutaneous abscesses
  • hidradenitis
View approved original text

This medication acts effectively against various bacterial infections, exhibiting antibacterial activity against several bacteria including Staphylococcus, Streptococcus, Streptococcus pneumoniae, Neisseria gonorrhoeae, Escherichia coli, etc. It is used for skin and soft tissue infections, such as folliculitis, furuncles, abscesses, cellulitis, lymphangitis, and paronychia. It is also effective in treating infections of the respiratory tract, including pharyngitis, acute and chronic bronchitis, and pneumonia. Additionally, it applies to urinary infections such as pyelonephritis and cystitis, as well as otitis media, sinusitis, and tonsillitis. It can be used for various infection sites including mastitis, Bartholin's gland inflammation, and perianal abscesses. Overall, this medication treats various types of bacterial infections, improving symptoms and aiding in recovery.

How to take

Adult dose

○ Adults: The usual oral dose is 100mg (potency) of cefpodoxime per dose, twice daily after meals. For severe cases or when the response is considered insufficient, the usual oral dose is 200mg (potency) per dose, twice daily after meals. The dose may be adjusted as appropriate according to age, symptoms, etc.

Child dose

○ Infants and children: Administer orally after reconstituting before use. The usual dose is 3mg (potency) of cefpodoxime per Kg of body weight per dose, 2~3 times daily. ○ Infants and children: For severe cases or cases in which the response is considered insufficient, administer 4.5mg (potency) per Kg of body weight per dose orally, 3 times daily. The dose may be adjusted as appropriate according to age, symptoms, etc.

Precautions

This medication should not be used in patients with a history of allergic reactions or shock. Additionally, it should not be administered to patients with lactose intolerance or certain genetic metabolic disorders. Patients with hypersensitivity to this medication or those allergic to cephalosporin antibiotics should use it cautiously and only in special situations. Individuals with allergies to penicillin antibiotics, asthma, or skin rash need to be cautious. Patients with severely impaired kidney function should be careful as this medication may not be well excreted, increasing the risk of side effects. Patients who have difficulty taking medication orally, elderly individuals, and those in poor general condition should be closely monitored for potential side effects such as vitamin K deficiency. This medication can rarely lead to severe allergic reactions, skin rashes, gastrointestinal disturbances, pneumonia, blood abnormalities, neurological disorders, liver dysfunction, or kidney abnormalities; thus, if any unusual symptoms occur, usage should be immediately stopped and medical consultation sought. It is important to administer this medication only for the minimum necessary duration to prevent the development of antibiotic-resistant bacteria. Before administration, it is recommended to conduct a thorough medical history to predict allergic reactions and perform skin reaction tests. Dizziness may occur while taking this medication, so caution is advised when driving or operating machinery. For prolonged administration of more than 10 days, it is necessary to check white blood cell counts through blood tests. In patients with reduced kidney function, dosage adjustments may be needed, and if neurological symptoms such as seizures occur, administration should be stopped immediately. Severe skin adverse reactions have been reported, so the condition of the skin should be closely monitored, and any abnormalities should be reported to medical personnel promptly. This medication may impose a burden on the kidneys when used with certain diuretics or antibiotics, so it should be used carefully in combination. Additionally, interactions with other drugs may alter drug concentrations; therefore, it is crucial to inform your healthcare provider of any other medications you are taking. Women who are pregnant or may become pregnant should use this medication cautiously only when necessary, and it is safe to discontinue breastfeeding while on this medication. Children, especially newborns or premature infants, should be used with caution as the safety of this medication has not been established in this population. The elderly should monitor dosages and intervals due to risks associated with bodily function decline and vitamin K deficiency-related bleeding. This medication may impact the results of some clinical tests, so it’s advisable to inform the healthcare provider during examinations. Syrup forms should be stored in a refrigerator after preparation and used within two weeks, shaking well before administration.

Side effects

shock

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

Storage

This medication should be stored in a tightly sealed container to prevent contact with light and air, preferably at room temperature between 1 degree and 30 degrees Celsius. Proper storage can maintain the drug's effectiveness for a long time.

Appearance and packaging

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 200 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.

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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.