Medication info

Lopam Tablet (Famciclovir)

Prescription medicationExpired
Ingredient · strength
Famciclovir›Strength being verified
Manufacturer / importer
IntroBioPharma Co., Ltd.
Appearance
White round film-coated tablet
Packaging
21 tablets (3 PTP of 7 tablets each)
Approval status
Expired

MFDS item code 201801084 · Approved 2018.03.08

This product's status changed to Expired on 2023.03.08. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of shingles; treatment and suppression of recurrence of genital herpes
Who uses it
Adults
Adult dosage
1. Treatment of herpes zoster Adults: Administer famciclovir 250 mg orally 3 times daily for 7 days. It is advisable to start treatment as soon as symptoms appear after infection. 2. Treatment of initial genital herpes infection Adults: Administer this drug 250 mg orally 3 times daily for 5 days. It is advisable to start treatment as soon as symptoms appear after infection. 3. Treatment of acute recurrent genital herpes infection Adults: Administer this drug 125 mg orally 2 times daily for 5 days. It is advisable to start treatment during the prodromal period or as soon as symptoms appear after infection. 4. Suppression of recurrent genital herpes Adults: Administer this drug 250 mg orally 2 times daily. Interrupt treatment periodically every 6~12 months to assess whether the natural course of the disease has changed. 5. Patients with renal impairment: Because the clearance of this drug decreases in patients with renal impairment, dosage adjustment should be undertaken with caution. The dosage and administration for these patients are as follows. 1) Treatment of herpes zoster and initial genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 250 mg per dose, 2 times daily 10~29: 250 mg per dose, once daily 2) Treatment of acute recurrent genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 125 mg per dose, 2 times daily 10~29: 125 mg per dose, once daily 3) Suppression of recurrent genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 250 mg per dose, 2 times daily 10~29: 125 mg per dose, 2 times daily 4) If only serum creatinine is known, creatinine clearance may be calculated using the following equations. Men: {body weight (kg) × (140-age)}/ {72 × serum creatinine (mg/dL)} Women: 0.85 × the value calculated for men 5) Patients with renal impairment undergoing hemodialysis For patients undergoing hemodialysis, administration every 48 hours is advisable, taking the interval between dialysis sessions into consideration. Since 4 hours of hemodialysis reduces the plasma concentration of this drug by approximately 75%, administer this drug immediately after dialysis. The recommended dose is 250mg for patients with herpes zoster and 125mg for patients with genital herpes. 6. Patients with hepatic impairment: No dosage adjustment is necessary in patients with chronic compensated liver disease. Since there is insufficient treatment experience in patients with overt chronic decompensated liver disease, a clear recommended dosage has not been established.

Ingredients

Manufacturer
IntroBioPharma Co., Ltd.

Efficacy & effects

Treatment of shingles; treatment and suppression of recurrence of genital herpes

  • Herpes zoster virus infection
  • genital herpes infection
  • recurrent genital herpes
View approved original text

This medication is used for the treatment of herpes zoster virus infections and genital herpes infections. It also helps to suppress the recurrence of recurrent genital herpes.

Dosage and Administration

Adult dosage

1. Treatment of herpes zoster Adults: Administer famciclovir 250 mg orally 3 times daily for 7 days. It is advisable to start treatment as soon as symptoms appear after infection. 2. Treatment of initial genital herpes infection Adults: Administer this drug 250 mg orally 3 times daily for 5 days. It is advisable to start treatment as soon as symptoms appear after infection. 3. Treatment of acute recurrent genital herpes infection Adults: Administer this drug 125 mg orally 2 times daily for 5 days. It is advisable to start treatment during the prodromal period or as soon as symptoms appear after infection. 4. Suppression of recurrent genital herpes Adults: Administer this drug 250 mg orally 2 times daily. Interrupt treatment periodically every 6~12 months to assess whether the natural course of the disease has changed. 5. Patients with renal impairment: Because the clearance of this drug decreases in patients with renal impairment, dosage adjustment should be undertaken with caution. The dosage and administration for these patients are as follows. 1) Treatment of herpes zoster and initial genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 250 mg per dose, 2 times daily 10~29: 250 mg per dose, once daily 2) Treatment of acute recurrent genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 125 mg per dose, 2 times daily 10~29: 125 mg per dose, once daily 3) Suppression of recurrent genital herpes infection: Creatinine clearance (mL/min/1.73㎡) 30~59: 250 mg per dose, 2 times daily 10~29: 125 mg per dose, 2 times daily 4) If only serum creatinine is known, creatinine clearance may be calculated using the following equations. Men: {body weight (kg) × (140-age)}/ {72 × serum creatinine (mg/dL)} Women: 0.85 × the value calculated for men 5) Patients with renal impairment undergoing hemodialysis For patients undergoing hemodialysis, administration every 48 hours is advisable, taking the interval between dialysis sessions into consideration. Since 4 hours of hemodialysis reduces the plasma concentration of this drug by approximately 75%, administer this drug immediately after dialysis. The recommended dose is 250mg for patients with herpes zoster and 125mg for patients with genital herpes. 6. Patients with hepatic impairment: No dosage adjustment is necessary in patients with chronic compensated liver disease. Since there is insufficient treatment experience in patients with overt chronic decompensated liver disease, a clear recommended dosage has not been established.

Precautions

This medication should not be used by patients who are allergic to certain ingredients. Additionally, since it contains lactose, it should not be administered to patients with lactose intolerance or specific genetic metabolic disorders. Caution is needed when using this medication in patients with impaired kidney function, and dose adjustments may be necessary. This medication may cause symptoms such as headache or nausea, but they are generally mild. Rarely, side effects such as decreased blood cell counts, hallucinations, palpitations, or skin rashes may occur, so if symptoms arise, consult a doctor immediately. This medication does not completely treat genital herpes, so it is important to avoid sexual contact when symptoms are present and to maintain safe sex practices. If symptoms such as dizziness or drowsiness occur while taking this medication, it is advised to refrain from driving or operating machinery. Patients with slightly reduced liver function do not require special dose adjustments, but patients with severe liver impairment may experience reduced efficacy. This medication does not have significant interactions with other drugs, but blood concentration changes may need to be monitored when used with some medications. Pregnant or breastfeeding women should use this medication cautiously and consult a doctor, as its safety during pregnancy has not been fully established. Use in children under 18 years is not recommended due to lack of established safety and efficacy. Elderly patients generally do not need dose adjustments, but dose adjustments should be made if kidney function is impaired. In case of overdose, hemodialysis may be helpful, and immediate treatment is required. This medication should be stored in a cool, dry place away from direct sunlight and kept out of reach of children.

Side effects

  • headache
  • nausea
  • thrombocytopenia
  • leukopenia
  • neutropenia
  • dizziness
  • confusion
  • drowsiness
  • hallucination
  • palpitations
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  • vomiting
  • abdominal pain
  • diarrhea
  • abnormal liver function test
  • jaundice
  • skin rash
  • itching
  • urticaria
  • angioedema
  • acute renal failure
  • upper abdominal pain
  • constipation
  • liver dysfunction
  • diarrhea
  • abdominal bloating
  • dyspepsia
  • facial swelling
  • fatigue
  • pain
  • leukopenia
  • insomnia
  • shortened menstrual period
  • urinary difficulty

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 exposure to air or moisture, preferably in a dry place at temperatures below 30 degrees Celsius. Storing it this way can help maintain the effectiveness of the medication for a longer period.

Appearance and packaging

Appearance

White round film-coated tablet

Package unit

21 tablets (3 PTP of 7 tablets each)

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.