250.00

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Information on this page was last modified on : 2021/05/20 8:50:23 PM

Dermoflam 1.00% Cream Jarx250 gm

Belongs to Category

Dermoflam Cream contains Silver Sulphadiazine | belongs to Antibacterial

Alternate brands of Dermoflam 1.00% Cream Jarx250 gm

Brand Name Price Savings
Xeburn 1.00% Cream Jarx250 gm  200.00 You can save 50
Xeburn 1.00% Cream Jarx20 gm  72.00 You can save 178
Vee-Burna-Fax 1.00% Cream Jarx500 gm  532.00 You will pay -282 more
Vee-Burna-Fax 1.00% Cream Jarx250 gm  296.00 You will pay -46 more
Vee-Burna-Fax 1.00% Cream Jarx50 gm  74.00 You can save 176
List of alternate brands

How it works

This medicine acts on the cell wall and cell membrane of the bacteria to cause their death.

Side effects

Major & minor side effects for Dermoflam 1.00% Cream Jarx250 gm

  • Burning sensation at the application site
  • Itching of skin
  • Skin rash
  • Yellowing of skin and eyes
  • Redness of skin
  • Dark colored urine

Uses of Dermoflam 1.00% Cream Jarx250 gm

What is it prescribed for?

  • Burn wound infections

    This medicine is used for the prevention and treatment of wound infections in patients with second and third-degree burns.

Concerns

Frequently asked questions

  • Onset of action

    The amount of time required for this medicine to show its action is not clinically established.

  • Duration of Effect

    The amount of time for which this medicine remains active in the body is not clinically established.

  • Safe with Alchohol?

    Interaction with alcohol is unknown. It is advisable to consult your doctor before consumption.

  • Is it habit forming?

    No habit forming tendency has been reported.

  • Usage in pregnancy?

    This medicine is not recommended for use in pregnant women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before using this medicine.

  • Usage while breast-feeding?

    This medicine is not recommended for use in breastfeeding women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before using this medicine. Your doctor may advise you to discontinue breastfeeding or to discontinue the drug based on your clinical condition.

When not to use?

  • Allergy

    This medicine is not recommended for use in patients with a known allergy to silver sulfadiazine, silver, or any other inactive ingredients present along with it.

Warnings

Warnings for special population
  • Pregnancy

    This medicine is not recommended for use in pregnant women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before using this medicine.

  • Breast-feeding

    This medicine is not recommended for use in breastfeeding women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before using this medicine. Your doctor may advise you to discontinue breastfeeding or to discontinue the drug based on your clinical condition.

General Warnings
  • Hypersensitivity reactions

    This medicine should be used with caution in patients with severe allergies, bronchial asthma, or AIDS due to the increased risk of severe hypersensitivity reactions. Report any unusual symptoms to the doctor immediately. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • Crystalluria

    Use of this medicine may cause crystalluria due to the precipitation of this medicine in the urinary tract. This risk is especially higher in patients suffering from dehydration. Patients are advised to drink an adequate amount of water during treatment with this medicine. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency

    This medicine should be used with extreme caution in patients with Glucose-6-phosphate dehydrogenase (G6PD) deficiency due to the increased risk of worsening of the patient's condition. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • Use in pediatrics

    This medicine is not recommended for use in patients less than 18 years of age.

Dosage

  • Missed Dose

    Use/apply the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose. Do not double your dose to make up for the missed one.

  • Overdose

    An overdose of this medicine is not likely to cause severe symptoms. However, ingestion of this medicine may cause harm and immediate medical intervention may be required.

Interactions

Interaction with Medicines
  • Sodium Nitrite severe
  • Prilocaine severe
  • Collagenase moderate
Disease interactions
  • severe

    This medicine should be used with extreme caution in patients with preexisting blood dyscrasias or bone marrow suppression due to the increased risk of worsening of the patient's condition. Report any signs or symptoms such as a fever, sore throat, local infection, bleeding, pallor, dizziness, or jaundice to the doctor immediately. Close monitoring of complete blood counts is recommended for such patients. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • severe

    This medicine should be used with caution in patients suffering from porphyria due to the increased risk of worsening of the patient's condition. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • moderate

    This medicine should be used with caution in patients with liver impairment due to the increased risk of severe adverse effects. Close monitoring of liver function may be required while using this medicine. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

  • moderate

    This medicine should be used with caution in patients with renal impairment due to the increased risk of severe adverse effects. Close monitoring of renal function may be required while using this medicine. Replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

Lab interactions

General Instructions

This medicine is meant for external use only. If the medicine is swallowed, seek immediate medical help. Follow all dosing instructions mentioned on the label or the package insert. Do not use this medicine for durations shorter or longer than recommended by your doctor. Ensure that the treatment course is completed. Report any undesired side effects to the doctor immediately. Do not stop the use of this medicine without consulting your doctor.

Other details

  • Usage does not depend on food timings
  • To be taken as instructed by doctor
  • Does not cause sleepiness

References

Additional Information:

What happens if I miss a dose of Dermoflam 1.00% Cream Jarx250 gm?

Adults: Apply in layer 3-5 mm thick. Change dressing three times a wk for ulcers and daily for burns. Children: Up to 3 mth, not recommended; others, same as adult.

One of the following licensed pharmacy from the nearest location will deliver Dermoflam 1.00% Cream Jarx250 gm. The details of the licensed pharmacy shall be shared once you request the drugs and the respective pharmacy accepts your request based on valid prescription and availability.

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