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Peflera tablet 400 mg 10's

Belongs to Category,

Peflera tablet contains Pefloxacin | belongs to Quinolone

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How it works

Peflera tablet 400 mg 10’s blocks the multiplication and growth of bacteria; this results in the eventual death of the bacteria.

Side effects

Major & minor side effects for Peflera tablet 400 mg 10’s

  • Difficulty in falling or staying asleep
  • Dizziness
  • Headache
  • Nausea
  • Vomiting
  • Diarrhea
  • Itching

Uses of Peflera tablet 400 mg 10’s

What is it prescribed for?

  • Bacterial infections

    This medicine is used in the treatment of various infections caused by gram-negative bacteria and Staphylococci strains.

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 tendencies were 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 taking/receiving this medicine. Your doctor may prescribe a safer alternative based on your clinical condition.

  • 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 taking/receiving 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 Peflera tablet 400 mg 10’s , any other fluoroquinolones, or any other inactive ingredients present along with it.

  • Tendinitis or tendon rupture

    This medicine is not recommended for use in patients with a known history of tendon rupture or tendinitis (a condition in which the tissue connecting muscles to the bones becomes inflamed) due to the increased risk of worsening of the patient's condition.

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 taking/receiving this medicine. Your doctor may prescribe a safer alternative based on your clinical condition.

  • 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 taking/receiving this medicine. Your doctor may advise you to discontinue breastfeeding or to discontinue the drug based on your clinical condition.

Warnings

Warnings for special population
  • Tendinitis or tendon rupture

    Use of this medicine will increase the risk of tendinitis or tendon rupture during the treatment or several months after the treatment. This may affect your shoulders, hands, ankles, or other parts of your body. You are at a higher risk if you are more than 60 years of age or if you have undergone a transplant of kidney, heart, or lung. You are also at a higher risk if you are on corticosteroids such as dexamethasone, methylprednisolone, or prednisone. Report any unusual symptoms to the doctor immediately. Appropriate corrective measures, dose adjustments, or replacement with a suitable alternative may be required in some cases based on the clinical condition.

  • Drug-resistance

    Usage of this medicine without sufficient proof or suspicion of a bacterial infection should be avoided. Irrational dosing might fail in providing benefits and may even cause toxicity. It may also increase the risk of development of bacteria that are drug resistant.

  • Driving or Operating machinery

    Use of this medicine may cause symptoms such as confusion, dizziness, etc. in some patients. It is advised that you do not perform any activities such as driving a vehicle or operating machinery if you experience any of these symptoms during treatment with this medicine.

  • Photosensitivity

    This medicine may make you more sensitive to sunlight or tanning lights. You are advised to use sunscreen and wear protective clothing to avoid adverse reactions to sunlight during treatment with this medicine.

  • This medicine may make you more sensitive to sunlight or tanning lights. You are advised to use sunscreen and wear protective clothing to avoid adverse reactions to sunlight during treatment with this medicine.

    This medicine is not recommended for use in patients less than 12 years of age due to the increased risk of serious adverse effects.

  • Intravenous administration

    The injection form of this medicine should be infused intravenously over a duration of at least 60 minutes.

Dosage

  • Missed Dose

    Oral form: Take 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. Injection: Since this medicine is administered in the hospital or clinical setting by a qualified healthcare professional, the likelihood of a missed dose is very low.

  • Overdose

    Oral: Seek emergency medical treatment or contact the doctor in case of an overdose. Injection: Since this medicine is administered in the hospital or clinical setting by a qualified healthcare professional, the likelihood of an overdose is very low. However, emergency medical treatment will be initiated by the doctor if an overdose is suspected.

Interactions

Interaction with Medicines
  • Corticosteroids
  • Antidiabetic drugs
  • Antacids
  • Anticoagulants
  • Theophylline
Disease interactions
  • This medicine should be used with extreme caution in patients with a history of seizure disorder and other central nervous system abnormalities since it may worsen the patient's condition. Report any incidence of tremors, restlessness, anxiety, confusion, hallucinations, etc., to the doctor on priority. Appropriate dose adjustments or replacement with a suitable alternative may be required in some cases based on the clinical condition of the patient.

  • This medicine should be used with caution in patients with a known history of liver impairment since it may worsen the patient's condition. Report any unusual symptoms to the doctor on priority. Close monitoring of liver function is necessary while receiving this medicine. Appropriate dose adjustments or replacement with a suitable alternative may be required in some cases based on the clinical condition.

Lab interactions

General Instructions

Oral form: Take this medicine with food. Do not take in larger or smaller amounts than advised/prescribed. Consult the doctor if you experience any undesirable side effects. Ensure that the treatment course is completed. Do not stop the use of this medicine without consulting your doctor. Injection: This medicine should be administered by a qualified healthcare professional. Inform the doctor if you have a known history of allergy to this medicine. Report to the doctor all your current medicines as well as your medical conditions before receiving this medicine.

Other details

  • To be taken with food
  • To be taken as instructed by doctor
  • May cause sleepiness

References

How to use Peflera tablet 400 mg 10’s

Adults: 400 mg in D5W (250 mL), administered by slow IV infusion over 1 hr twice daily.

what are the adverse effects of Peflera tablet 400 mg 10’s

Gl upset, headache, insomnia, pain in muscles and joint.

What is the dose of Peflera tablet 400 mg 10’s

ORAL/IV INFUSION: Adults: 400 mg twice daily. Children: Not recommended.

One of the following licensed pharmacy from the nearest location will deliver Peflera tablet 400 mg 10’s. The details of the licensed pharmacy shall be shared once you request the drugs and the respective pharmacy accepts the your request based on valid prescription and availability.

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