Cefditoren: Difference between revisions
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==General== | ==General== | ||
*Type: | *Type: [[Is Generation::3rd generation]] [[Is DrugClass::cephalosporin]] | ||
*Dosage Forms: | *Dosage Forms: tablet | ||
*Common Trade Names: | *Dosage Strengths: 200, 400mg | ||
*Routes of Administration: PO | |||
*Common Trade Names: Spectracef | |||
==Adult Dosing== | ==Adult Dosing== | ||
===Chronic [[Bronchitis]], Acute bacterial exacerbation=== | |||
*400 mg PO bid x10 days | |||
===[[Pneumonia]], community-acquired=== | |||
*400 mg PO bid for at least 5 days | |||
**May D/C after five days if afebrile x48-72 hours | |||
===[[Pharyngitis]]/Tonsillitis, streptococcal=== | |||
*200mg PO bid x10 days | |||
===Skin infection=== | |||
*200 mg PO bid x10 days | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===12+ yo, Chronic [[Bronchitis]], Acute bacterial exacerbation=== | |||
*400 mg PO bid x10 days | |||
===12+ yo, [[Pneumonia]], community-acquired=== | |||
*400 mg PO bid x14 days | |||
===12+ yo, [[Pharyngitis]]/Tonsillitis, streptococcal=== | |||
*200mg PO bid x10 days | |||
===12+ yo, Skin infection=== | |||
*200 mg PO bid x10 days | |||
==Special Populations== | ==Special Populations== | ||
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: | *[[Drug Ratings in Pregnancy|Pregnancy Rating]]: B; May use during pregnancy | ||
*Lactation: | *Lactation: May use while breastfeeding | ||
*Renal Dosing | *Renal Dosing | ||
**Adult | **Adult | ||
***CrCl 30-49: Max 200mg bid | |||
***CrCl <30: Max 200mg qd | |||
***ESRD/HD: Not defined | |||
**Pediatric | **Pediatric | ||
***CrCl 30-49: Max 200mg bid | |||
***CrCl <30: Max 200mg qd | |||
***ESRD/HD: Not defined | |||
*Hepatic Dosing | *Hepatic Dosing | ||
**Adult | **Adult | ||
***Child-Pugh Class A or B: No adjusment | |||
***Child-Pugh Class C: Not defined | |||
**Pediatric | **Pediatric | ||
***Child-Pugh Class A or B: No adjusment | |||
***Child-Pugh Class C: Not defined | |||
==Contraindications== | ==Contraindications== | ||
*Allergy to class/drug | *Allergy to class/drug | ||
*Hypersensitivity to milk proteins | |||
*Carnitine deficiency | |||
*Caution: | |||
**Hypersensitivity to PCN | |||
**Renal impairment | |||
**Decreased muscle mass | |||
**Recent abx-associated colitis | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*[[Anaphylaxis]] | |||
*Serum-sickness like reaction | |||
*[[Stevens-Johnson syndrome]] | |||
*[[Erythema multiforme]] | |||
*[[Toxic epidermal necrolysis]] | |||
*[[Leukopenia]] | |||
*[[Neutropenia]] | |||
*[[Thrombocytopenia]] | |||
*[[Anemia]], hemolytic | |||
*[[Seizure]] | |||
*Nephrotoxicity | |||
*Cholestatic [[jaundice]] | |||
*C. difficle-associated diarrhea | |||
*Super infection | |||
*Carnitine deficiency (long-term use) | |||
===Common=== | ===Common=== | ||
*[[Diarrhea]] | |||
*[[Nausea]] | |||
*[[Headache]] | |||
*[[Abdominal pain]] | |||
*Candidiasis, vulvovaginal | |||
*Dyspepsia | |||
==Pharmacology== | ==Pharmacology== | ||
*Half-life: | *Half-life: 1.6h; 4.7h in severe renal impairment | ||
*Metabolism: | *Metabolism: Minimal | ||
*Excretion: | *Excretion: Urine primarily | ||
*Mechanism of Action: | *Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis | ||
==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ==[[Antibiotic Sensitivities]]<ref>Sanford Guide to Antimicrobial Therapy 2014</ref>== | ||
| Line 157: | Line 214: | ||
*[[Antibiotics (Main)]] | *[[Antibiotics (Main)]] | ||
== | ==References== | ||
<references/> | |||
[[Category:Pharmacology]] [[Category:ID]] | |||
[[Category:Pharmacology]] | |||
Latest revision as of 16:20, 18 July 2025
General
- Type: 3rd generation cephalosporin
- Dosage Forms: tablet
- Dosage Strengths: 200, 400mg
- Routes of Administration: PO
- Common Trade Names: Spectracef
Adult Dosing
Chronic Bronchitis, Acute bacterial exacerbation
- 400 mg PO bid x10 days
Pneumonia, community-acquired
- 400 mg PO bid for at least 5 days
- May D/C after five days if afebrile x48-72 hours
Pharyngitis/Tonsillitis, streptococcal
- 200mg PO bid x10 days
Skin infection
- 200 mg PO bid x10 days
Pediatric Dosing
12+ yo, Chronic Bronchitis, Acute bacterial exacerbation
- 400 mg PO bid x10 days
12+ yo, Pneumonia, community-acquired
- 400 mg PO bid x14 days
12+ yo, Pharyngitis/Tonsillitis, streptococcal
- 200mg PO bid x10 days
12+ yo, Skin infection
- 200 mg PO bid x10 days
Special Populations
- Pregnancy Rating: B; May use during pregnancy
- Lactation: May use while breastfeeding
- Renal Dosing
- Adult
- CrCl 30-49: Max 200mg bid
- CrCl <30: Max 200mg qd
- ESRD/HD: Not defined
- Pediatric
- CrCl 30-49: Max 200mg bid
- CrCl <30: Max 200mg qd
- ESRD/HD: Not defined
- Adult
- Hepatic Dosing
- Adult
- Child-Pugh Class A or B: No adjusment
- Child-Pugh Class C: Not defined
- Pediatric
- Child-Pugh Class A or B: No adjusment
- Child-Pugh Class C: Not defined
- Adult
Contraindications
- Allergy to class/drug
- Hypersensitivity to milk proteins
- Carnitine deficiency
- Caution:
- Hypersensitivity to PCN
- Renal impairment
- Decreased muscle mass
- Recent abx-associated colitis
Adverse Reactions
Serious
- Anaphylaxis
- Serum-sickness like reaction
- Stevens-Johnson syndrome
- Erythema multiforme
- Toxic epidermal necrolysis
- Leukopenia
- Neutropenia
- Thrombocytopenia
- Anemia, hemolytic
- Seizure
- Nephrotoxicity
- Cholestatic jaundice
- C. difficle-associated diarrhea
- Super infection
- Carnitine deficiency (long-term use)
Common
- Diarrhea
- Nausea
- Headache
- Abdominal pain
- Candidiasis, vulvovaginal
- Dyspepsia
Pharmacology
- Half-life: 1.6h; 4.7h in severe renal impairment
- Metabolism: Minimal
- Excretion: Urine primarily
- Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis
Antibiotic Sensitivities[1]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
See Also
References
- ↑ Sanford Guide to Antimicrobial Therapy 2014
