MIKAN 500mg Injection Vial

 280.90

Manufactured by:
Active Pharmaceutical Ingredient:
Drug Strength: 500mg
Drug Form : Injection
Pack Size : Vial
Does this requires a prescription ?Yes

Amikacin (Sulphate):500mg | Aminoglycosides

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    Manufactured / Marketed By : AGP Product Form : InjectionPack Size : VialIngredients : Amikacin (Sulphate):500mgGeneric Category : Aminoglycosides

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    How it works

    It interferes with the production of certain vital components necessary for the susceptible bacteria to grow and results in the eventual death of the bacteria.

    Side effects

    Major & minor side effects for MIKAN 500mg Injection Vial

    • Black or tarry stools severe
    • Blurred vision severe
    • Decrease in frequency of urination severe
    • Dizziness severe
    • Difficulty in breathing severe
    • Hearing loss severe
    • Muscle pain severe
    • Unusual tiredness and weakness severe
    • Skin Rash
    • Vomiting
    • Eyelid Edema
    • Eye pain
    • Visual disturbances
    • Corneal Scar
    • Dilated pupils

    Uses of MIKAN 500mg Injection Vial

    What is it prescribed for?

    • Intra-abdominal Infection

      This medicine is used in the treatment of intra-abdominal infections such as peritonitis, appendicitis, intra-abdominal abscess, etc. caused by bacteria such as E.coli, Streptococci, Enterococci, etc.

    • Pneumonia

      This medicine is used in the treatment of pneumonia, which is a common type of lung infection caused by bacteria such as Streptococcus pneumoniae, Haemophilus influenzae, etc.

    • Bacteremia

      This medicine is used in the treatment of bacteremia, which is an infection of the blood caused by Staphylococci, Streptococcus pyogenes, etc.

    • Bone and Joint infections

      This medicine is used in the treatment of bone and joint infections such as septic arthritis, osteomyelitis, etc. caused by Staphylococci and Streptococci species.

    • Bacterial Conjunctivitis

      This medicine is used in the treatment of conjunctivitis, an infection of the conjunctiva, caused by bacteria such as Haemophilus influenzae, Streptococcus pneumoniae, etc.

    • Bacterial Keratitis

      This medicine is used in the treatment of keratitis, an infection of the cornea, caused by bacteria such as Pseudomonas aeruginosa, Staphylococcus aureus, etc.

    • Blepharoconjunctivitis

      This medicine is used in the treatment of blepharoconjunctivitis, an inflammation or infection of the eyelids and conjunctiva, characterized by redness and discharge from the eye.

    • Strabismus Surgery

      This medicine is used after a strabismus (squint) surgery to prevent an infection of the eyes.

    Concerns

    Frequently asked questions

    • Onset of action

      The peak effect of this medicine can be observed within 45 to 120 minutes after intramuscular administration.

    • Duration of Effect

      The effect of this medicine lasts for an average duration of 8 to 12 hours.

    • 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 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 receiving this medicine. If the medicine is used, the infant should be monitored closely for any undesired side effects.

    When not to use?

    • Allergy

      This medicine is not recommended for use in patients with a known allergy to MIKAN 500mg Injection Vial, any other aminoglycosides, or any other inactive ingredients present along with it.

    • Impaired Kidney function

      The parenteral form (injection) of this medicine is not recommended for use in patients with a known history of renal impairment 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 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 receiving this medicine. If the medicine is used, the infant should be monitored closely for any undesired side effects.

    General Warnings
    • Allergy

      This medicine is not recommended for use in patients with a known allergy to MIKAN 500mg Injection Vial or any other aminoglycosides. Seek immediate medical attention if you experience any allergic symptoms such as a rash, itching, nausea or vomiting, swelling of lips, hands, and feet, etc.

    • Drug-resistance

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

    • Impaired kidney function

      This medicine should be used with extreme caution in patients with kidney diseases due to the increased risk of worsening of the patient's condition. Close monitoring of kidney function, appropriate dose adjustments, or replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

    • Myasthenia gravis

      This medicine should be used with extreme caution in patients with a history of myasthenia gravis due to the increased risk of worsening of the patient's condition. Any unusual symptoms should be reported to the doctor on priority. Replacement with a suitable alternative may be necessary in some cases based on the clinical condition.

    • Pediatric use

      Caution is advised while using this medicine in pediatric patients due to the increased risk of kidney injuries.

    • Driving or Operating machinery

      Use of this medicine may cause symptoms such as dizziness, drowsiness, blurred vision, 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.

    • Intravenous Administration

      This medicine should be administered only by a slow intravenous infusion over a period of 30 to 60 minutes for adults and adolescents. Infants should be infused over a duration of 1 to 2 hours.

    • Contact Lens

      While using the ophthalmic form of this medicine, usage of contact lens is not recommended if any signs and symptoms of an eye infection such as eye redness, irritation, drainage, etc. are present.

    Dosage

    • Missed Dose

      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. Eye Drops: Administer the missed dose as soon as you remember. It is advisable to skip the missed dose if it is almost time for your next scheduled dose. Do not instill a double dose to make up for the missed one.

    • 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. Eye Drops: The likelihood of an overdose with the ophthalmic form of this medicine is very low. However, seek emergency medical treatment or contact the doctor if you suspect an overdose of this medicine.

    Interactions

    Interaction with Medicines
    • Ceftriaxone moderate
    • Ethinyl Estradiol moderate
    • Furosemide severe
    • Aspirin moderate
    • Adefovir severe
    Disease interactions
    • severe

      This medicine should be used with caution in patients with a known history of disorders such as myasthenia gravis or parkinsonism due to the increased risk of worsening of the patient's condition. An alternative treatment option should be considered based on the clinical condition.

    • severe

      This medicine should be used with extreme caution in patients with kidney diseases or patients undergoing treatment with NSAIDs for a long time due to the increased risk of worsening of the patient's condition. Close monitoring of kidney function, appropriate dose adjustments, or replacement with a suitable alternative may be necessary based on the clinical condition of the patient.

    General Instructions

    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. Eye Drops: Use this medicine exactly as prescribed. Do not administer 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.

    Other details

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

    References

    Additional Information>

    One of the following licensed pharmacy from the nearest location will deliver MIKAN 500mg Injection Vial. 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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