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Buy Acnifen

500 mg, 250 mg

Acnifen gel 500 mg, 250 mg image

Active ingredient: erythromycin

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Categories of AcnifenAntibiotics
Average price (USD)$0.47
Manufacturer country (Worldwide Sale)Peru
Medication ClassMacrolides

Acnifen medications over the counter

There have been published reports Using this when oral for example is given concurrently with ingredient there is a significant decrease in erythromycin serum concentrations. Erythromycin significantly alters the active ingredient of terfenadine, astemizole and pimozide when taken concomitantly. Because of the possibility for adverse reactions in nursing infants from erythromycin, a choice should be made whether to stop nursing or to stop use of this medication. Drugs in the erythromycin group may be used to eliminate such areas of infection as abscesses prior to surgery.

Side Effects

Possible side effects of Acnifen include:

  • unusual tiredness or weakness
  • dark urine
  • red skin lesions, often with a purple center
  • bloody or cloudy urine

Used for

Acnifen is used to treat diseases such as: Bacterial Endocarditis Prevention, Bartonellosis, Bowel Preparation, Bronchitis, Bullous Pemphigoid, Campylobacter Gastroenteritis, Chancroid, Chlamydia Infection, Dental Abscess, Legionella Pneumonia, Lyme Disease, Lymphogranuloma Venereum, Mycoplasma Pneumonia, Nongonococcal Urethritis, Ocular Rosacea, Otitis Media, Pemphigoid, Pertussis, Pharyngitis, Pneumonia, Rheumatic Fever Prophylaxis, Skin or Soft Tissue Infection, Strep Throat, Syphilis, Early, Upper Respiratory Tract Infection.

How to Use

  • Follow the directions on your prescription or product label carefully, and ask your doctor or pharmacist to explain any part you do not understand.
  • Not if you follow the directions to apply it.

Dosage & Overdose

To treat ulcers in the stomach, reflux esophagitis, and ulcers associated with the use of NSAIDs, the recommended adult dose is 20 mg taken once daily for 4 to 8 weeks. With higher daily doses, toxicity can occur rapidly, even within the first 2 weeks of therapy.


  • Details of the serious adverse events and deaths in all treatment groups are provided in Table S5 in the Supplementary Appendix.