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Cefdinir

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Overview

What is Cefdinir?



What does Cefdinir look like?



What are the available doses of Cefdinir?

Sorry No records found.

What should I talk to my health care provider before I take Cefdinir?

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How should I use Cefdinir?

INDICATIONS AND USAGE


What interacts with Cefdinir?

Sorry No Records found


What are the warnings of Cefdinir?

Sorry No Records found


What are the precautions of Cefdinir?

General

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DOSAGE AND ADMINISTRATION

Information for Patients

Drug Interactions

Drug/Laboratory Test Interactions

Carcinogenesis, Mutagenesis, Impairment of Fertility

in vitro

in vivo

Pregnancy

Labor and Delivery

Nursing Mothers

Pediatric Use

Geriatric Use

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DOSAGE AND ADMINISTRATION


What are the side effects of Cefdinir?

Clinical Trials – Cefdinir Capsules (Adult and Adolescent Patients)

a
   Incidence ≥1%    Diarrhea 15%
   Vaginal moniliasis    4% of Women   
   Nausea 3%
   Headache 2%
   Abdominal pain 1%
   Vaginitis    1% of Women   
   Incidence <1% but >0.1%       Rash 0.9%
   Dyspepsia 0.7%
   Flatulence 0.7%
   Vomiting 0.7%
   Abnormal stools 0.3%
   Anorexia 0.3%
   Constipation 0.3%
   Dizziness 0.3%
   Dry mouth 0.3%
   Asthenia 0.2%
   Insomnia 0.2%
   Leukorrhea    0.2% of Women   
   Moniliasis 0.2%
   Pruritus 0.2%
   Somnolence 0.2%
 a
   Incidence ≥1%    ↑Urine leukocytes 2%
   ↑Urine protein 2%
   ↑Gamma-glutamyltransferase 1%
   ↓Lymphocytes, ↑Lymphocytes       1%, 0.2%   
   ↑Microhematuria 1%
   Incidence <1% but >0.1%       ↑Glucose 0.9%
   ↑Urine glucose 0.9%
   ↑White blood cells, ↓White blood cells    0.9%, 0.7%   
   ↑Alanine aminotransferase (ALT) 0.7%
   ↑Eosinophils 0.7%
   ↑Urine specific gravity, ↓Urine specific gravity    0.6%, 0.2%   
   ↓Bicarbonate 0.6%
   ↑Phosphorus, ↓Phosphorus    0.6%, 0.3%   
   ↑Aspartate aminotransferase (AST)    0.4%
   ↑Alkaline phosphatase 0.3%
   ↑Blood urea nitrogen (BUN) 0.3%
   ↓Hemoglobin 0.3%
   ↑Polymorphonuclear neutrophils (PMNs), ↓PMNs    0.3%, 0.2%
   ↑Bilirubin 0.2%
   ↑Lactate dehydrogenase 0.2%
   ↑Platelets 0.2%
   ↑Potassium 0.2%
   ↑Urine pH 0.2%


Clinical Trials - Cefdinir for Oral Suspension (Pediatric Patients)

Array
   Incidence ≥ 1%    Diarrhea 8%
   Rash 3%
   Vomiting 1%
   Incidence <1% but >0.1%       Cutaneous moniliasis 0.9%
   Abdominal pain 0.8%
   Leukopenia 0.3%
   Vaginal moniliasis    0.3% of girls   
   Vaginitis    0.3% of girls   
   Abnormal stools 0.2%
   Dyspepsia 0.2%
   Hyperkinesia 0.2%
   Increased AST 0.2%
   Maculopapular rash 0.2%
   Nausea 0.2%
a
   Incidence ≥1%    ↑Lymphocytes, ↓Lymphocytes    2%, 0.8%   
   ↑Alkaline phosphatase 1%
   ↓Bicarbonate 1%
   ↑Eosinophils 1%
   ↑Lactate dehydrogenase 1%
   ↑Platelets 1%
   ↑PMNs, ↓PMNs 1%, 1%
   ↑Urine protein 1%
   Incidence <1% but >0.1%       ↑Phosphorus, ↓Phosphorus    0.9%, 0.4%   
   ↑Urine pH 0.8%
   ↓White blood cells, ↑White blood cells    0.7%, 0.3%   
   ↓Calcium 0.5%
   ↓Hemoglobin 0.5%
   ↑Urine leukocytes 0.5%
   ↑Monocytes 0.4%
   ↑AST 0.3%
   ↑Potassium 0.3%
   ↑Urine specific gravity, ↓Urine specific gravity       0.3%, 0.1%   
   ↓Hematocrit 0.2%


Postmarketing Experience

Cephalosporin Class Adverse Events

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What should I look out for while using Cefdinir?

Sorry No records found


What might happen if I take too much Cefdinir?


How should I store and handle Cefdinir?

Store between 20-25°C (68-77°F); excursions permitted between 15-30°C (59-86°F).Do not refrigerate. Keep the bottle in the outer carton when not in use.The product should be used within three months after it has been opened.Store between 20-25°C (68-77°F); excursions permitted between 15-30°C (59-86°F).Do not refrigerate. Keep the bottle in the outer carton when not in use.The product should be used within three months after it has been opened.Store between 20-25°C (68-77°F); excursions permitted between 15-30°C (59-86°F).Do not refrigerate. Keep the bottle in the outer carton when not in use.The product should be used within three months after it has been opened.Enter section text here


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

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Interactions

Interactions

A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).