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ICONIR 125mg/5ml

Active Substance: Cefdinir.

51
UAD , based on 7541 reviews.
View Drug details
Overview

Welcome to Dwaey, specifically on ICONIR 125mg/5ml Powder for Suspension page.
This medicine contains an important and useful components, as it consists of Cefdinir.
ICONIR 125mg/5ml is available in the market in concentration 125 mg/5 ml and in the form of Powder for Suspension.

RETAJ PHARMACEUTICAL INDUSTRIES is the producer of ICONIR 125mg/5ml and it is imported from JORDAN, The most popular alternatives of ICONIR 125mg/5ml are listed downward .

Mode Of Action & Indication

Cefdinir binds to one or more of the penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell wall, thus inhibiting biosynthesis and arresting cell wall assembly resulting in bacterial cell death.

Indication
  • Community-acquired pneumonia
  • Susceptible infections
  • Sinusitis
  • Otitis media
  • Sore throat
  • Soft tissue infections
  • Respiratory tract infections
  • Acute Exacerbations of Chronic bronchitis
  • Acute Maxillary Sinusitis
Precaution

Penicillin-sensitive patients; superinfection; seizure; pseudomembranous colitis; pregnancy, lactation; renal or hepatic insufficiency. Lactation: Unknown whether drug is excreted in milk

Side Effects
  • >10% Diarrhea (8-15%) 1-10% Vaginal moniliasis (<4%)
  • Nausea (3%)
  • Rash (3%)
  • Headache (2%)
  • Increased urine leukocytes (2%)
  • Increased urine protein (1-2%)
  • Decreased lymphocytes (1%)
  • Glycosuria (1%)
  • Increased alkaline phosphatase (1%)
  • Increased eosinophils (1%)
  • Increased platelets (1%) Potentially Fatal: Anaphylaxis; renal and hepatic failure.
Alternatives Price List
  • OMNICEF 300UAD 137
  • OMNICEF 125mg/5mlUAD 67
  • OMNICEF 125mg/5mlUAD 128
  • MINOCET 300 mgUAD 55
  • MINOCET 125 mg/5 mlUAD 26
Contra indication

Hypersensitivity.

Pregnancy and lactation

Pregnancy category: B

Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Interaction

Concomitant admin w/ antacids or Fe supplements reduce the rate and extent of absorption. Admin w/ Fe supplements may cause reddish stools. Decreased renal elimination w/ probenecid.

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