Ceftriaxone Sodium interactions
Checked as Ceftriaxone in this data source.
Full monograph for Ceftriaxone SodiumCheck it against another medicine
Medicines
501 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Calcium Gluconate | Major | Others | Coadministration of ceftriaxone with calcium-containing solutions, even via different infusion lines, may cause precipitation of ceftriaxone-calcium salt… | 4 sources — open the full entry |
| Folinic Acid | Major | Others | Coadministration of ceftriaxone with calcium-containing solutions, even via different infusion lines, may cause precipitation of ceftriaxone-calcium salt… | 4 sources — open the full entry |
| Light kaolin + Silver sulfadiazine + Calcium gluconate + Butane propellant | Major | Others | Coadministration of ceftriaxone with calcium-containing solutions, even via different infusion lines, may cause precipitation of ceftriaxone-calcium salt… | 4 sources — open the full entry |
| Amikacin | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + Lidocaine | Moderate | Antagonism · Unknown | Limited, primarily in vitro, data suggest that chloramphenicol may antagonize the bactericidal activity of cephalosporins against certain clinical isolates of…3 documented mechanisms | 8 sources — open the full entry |
| Betamethasone + Clotrimazole + Gentamicin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Betamethasone + Neomycin Sulphate (Ophthalmic) | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Bumetanide | Moderate | Synergy | Limited data suggest that furosemide and possibly other loop diuretics may potentiate the nephrotoxicity of some cephalosporins. The exact mechanism of… | 9 sources — open the full entry |
| Chloramphenicol (Oral) | Moderate | Antagonism | Limited, primarily in vitro, data suggest that chloramphenicol may antagonize the bactericidal activity of cephalosporins against certain clinical isolates of… | 8 sources — open the full entry |
| Chloramphenicol + Lidocaine Hydrochloride | Moderate | Antagonism · Unknown | Limited, primarily in vitro, data suggest that chloramphenicol may antagonize the bactericidal activity of cephalosporins against certain clinical isolates of…2 documented mechanisms | 8 sources — open the full entry |
| Cinchocaine + Hydrocortisone + Framycetin + Esculin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Cinchocaine + Hydrocortisone + Neomycin + Esculin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Clobetasol Propionate + Neomycin Sulphate + Nystatin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Cyclosporine (Oral) | Moderate | Synergy | Limited data suggest that ceftriaxone may increase cyclosporine serum concentrations. Risk of cyclosporine-induced neurotoxicity and nephrotoxicity may be… | 14 sources — open the full entry |
| Cyproterone Acetate + Ethinyl Estradiol | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Dexamethasone + Chloramphenicol | Moderate | Antagonism · Unknown | Limited, primarily in vitro, data suggest that chloramphenicol may antagonize the bactericidal activity of cephalosporins against certain clinical isolates of…2 documented mechanisms | 8 sources — open the full entry |
| Dexamethasone + Neomycin + Glacial Acetic Acid | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Dexamethasone + Neomycin Sulphate + Polymyxin B Sulphate | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Dexamethasone + Tobramycin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Dienogest + Estradiol Valerate | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Estradiol | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol0.02 mg0.03 mg | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol + Levomefolate | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiolbasevaginal cream | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol + Dydrogesterone | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol Hemihydrate + Progesterone Micronized | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol Valerate | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Desogestrel0.02 mg0.03 mg | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Gestodene | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Levonorgestrel + Ferrous Fumarate | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Lynestrenol0.0375 mg0.05 mg | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Fluocinolone Acetonide + Neomycin Sulfate | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Fluormetholone + Neomycin Sulphate | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Fluorometholone + Gentamicin | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Furosemide | Moderate | Synergy | Limited data suggest that furosemide and possibly other loop diuretics may potentiate the nephrotoxicity of some cephalosporins. The exact mechanism of… | 9 sources — open the full entry |
| Furosemide + Spironolactone | Moderate | Synergy · Unknown | Limited data suggest that furosemide and possibly other loop diuretics may potentiate the nephrotoxicity of some cephalosporins. The exact mechanism of…2 documented mechanisms | 9 sources — open the full entry |
| Gentamicin + Hydrocortisone Acetate | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Gentamicin SulfateInjectionOphthalmic | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Gramacidin + Neomycin + Polymixin B | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Hydrocortisone + Neomycin Sulphate + Polymixin B | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…2 documented mechanisms | 40 sources — open the full entry |
| Hydrocortisone Acetate + Neomycin Sulphate | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Kanamycin | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Loteprednol Etabonate + Tobramycin | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Metronidazole + Neomycin Sulphate + Polymyxin B + Nystatin | Moderate | Synergy · Unknown | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported…3 documented mechanisms | 40 sources — open the full entry |
| Mycophenolate Mofetil | Moderate | Absorption | Theoretically, drugs that alter the gastrointestinal flora (e.g., antibiotics) may reduce the oral bioavailability of mycophenolic acid products. Some… | 3 sources — open the full entry |
| Mycophenolic acid | Moderate | Absorption | Theoretically, drugs that alter the gastrointestinal flora (e.g., antibiotics) may reduce the oral bioavailability of mycophenolic acid products. Some… | 3 sources — open the full entry |
| Neomycin Sulfate + Bacitracin Zinc | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Neomycin Sulfate + Bacitracin Zinc + Polymyxin B Sulfate | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Neomycin Sulphate + Polymyxin B Sulphate + Pramoxine | Moderate | Synergy | Coadministration of aminoglycosides and cephalosporins may increase the risk of nephrotoxicity. An increased incidence of nephrotoxicity has been reported… | 40 sources — open the full entry |
| Norgestrel + Ethinyl Estradiol + Ferrous Fumarate | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
Conditions
Conditions in which Ceftriaxone Sodium needs care, as documented in this source.
Colitis
MajorClostridioides difficile-associated diarrhea (CDAD), formerly pseudomembranous colitis, has been reported with almost all antibacterial drugs and may range from mild diarrhea to fatal colitis. The most common culprits include clindamycin and lincomycin. Antibacterial therapy alters the normal flora of the colon, leading to overgrowth of C difficile, whose toxins A and B contribute to CDAD development. Morbidity and mortality are increased with hypertoxin-producing strains of C difficile; these infections can be resistant to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea after antibacterial use. Since CDAD has been reported to occur more than 2 months after antibacterial use, careful medical history is necessary. Therapy with broad-spectrum antibacterials and other agents with significant antibacterial activity should be administered cautiously in patients with history of gastrointestinal disease, particularly colitis; pseudomembranous colitis (generally characterized by severe, persistent diarrhea and severe abdominal cramps, and sometimes associated with the passage of blood and mucus), if it occurs, may be more severe in these patients and may be associated with flares in underlying disease activity. Antibacterial drugs not directed against C difficile may need to be stopped if CDAD is suspected or confirmed. Appropriate fluid and electrolyte management, protein supplementation, antibacterial treatment of C difficile, and surgical evaluation should be started as clinically indicated.
31 sources
- "Product Information. Omnipen (ampicillin)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Ceftin (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Zinacef (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Cleocin (clindamycin)." Pharmacia and Upjohn (2002):
- "Product Information. Macrobid (nitrofurantoin)." Procter and Gamble Pharmaceuticals (2002):
- "Product Information. Macrodantin (nitrofurantoin)." Procter and Gamble Pharmaceuticals (2002):
- "Product Information. Amoxil (amoxicillin)." SmithKline Beecham (2001):
- "Product Information. Merrem (meropenem)." Astra-Zeneca Pharmaceuticals (2001):
Show all 31 sourcesShow fewer sources
- "Product Information. Coly-Mycin M Parenteral (colistimethate)." Parke-Davis (2001):
- "Product Information. Lincocin (lincomycin)." Pharmacia and Upjohn (2001):
- "Product Information. Cubicin (daptomycin)." Cubist Pharmaceuticals Inc (2003):
- "Product Information. Xifaxan (rifaximin)." Salix Pharmaceuticals (2004):
- "Product Information. Doribax (doripenem)." Ortho McNeil Pharmaceutical (2007):
- "Product Information. Penicillin G Procaine (procaine penicillin)." Monarch Pharmaceuticals Inc (2009):
- "Product Information. Vibativ (telavancin)." Theravance Inc (2009):
- "Product Information. Teflaro (ceftaroline)." Forest Pharmaceuticals (2010):
- "Product Information. Penicillin G Sodium (penicillin G sodium)." Sandoz Inc (2022):
- "Product Information. Dalvance (dalbavancin)." Durata Therapeutics, Inc. (2014):
- "Product Information. Orbactiv (oritavancin)." The Medicines Company (2014):
- "Product Information. Bicillin C-R (benzathine penicillin-procaine penicillin)." A-S Medication Solutions (2017):
- "Product Information. Baxdela (delafloxacin)." Melinta Therapeutics, Inc. (2017):
- "Product Information. Polymyxin B Sulfate (polymyxin B sulfate)." AuroMedics Pharma LLC (2022):
- "Product Information. Zemdri (plazomicin)." Achaogen (2018):
- "Product Information. Seysara (sarecycline)." Allergan Inc (2018):
- "Product Information. Nuzyra (omadacycline)." Paratek Pharmaceuticals, Inc. (2018):
- "Product Information. Aemcolo (rifamycin)." Aries Pharmaceuticals, Inc. (2018):
- "Product Information. Fetroja (cefiderocol)." Shionogi USA Inc (2019):
- "Product Information. Biaxin (clarithromycin)." AbbVie US LLC (2019):
- "Product Information. Zithromax (azithromycin)." Pfizer U.S. Pharmaceuticals Group (2021):
- "Product Information. E.E.S.-400 Filmtab (erythromycin)." Arbor Pharmaceuticals (2018):
- "Product Information. Priftin (rifapentine)." sanofi-aventis (2020):
Hyperbilirubinemia
MajorHyperbilirubinemic neonates, especially premature, should not be treated with ceftriaxone for injection. Studies have shown that ceftriaxone can displace bilirubin from its binding to serum albumin, leading to possible risk of bilirubin encephalopathy in these patients.
1 source
- "Product Information. Rocephin (ceftriaxone)." Roche Laboratories (2002):
Epilepsy
ModerateCephalosporins have been implicated in triggering seizures. Nonconvulsive status epilepticus (NCSE), encephalopathy, coma, asterixis, neuromuscular excitability, and myoclonia have been reported with cephalosporins particularly in patients with a history of epilepsy and/or when recommended dosages of cephalosporins were exceeded due to renal impairment. Adjust dosing based on creatinine clearance. Anticonvulsant therapy should be continued in patients with known seizure disorders. If CNS adverse reactions including seizures occur, patients should undergo a neurological evaluation to determine whether treatment should be discontinued.
19 sources
- "Product Information. Vantin (cefpodoxime)." Pharmacia and Upjohn
- "Product Information. Ceclor (cefaclor)." Lilly, Eli and Company (2002):
- "Product Information. Duricef (cefadroxil)." Bristol-Myers Squibb (2002):
- "Product Information. Ancef (cefazolin)." SmithKline Beecham (2002):
- "Product Information. Kefzol (cefazolin)." Lilly, Eli and Company (2002):
- "Product Information. Suprax (cefixime)." Lupin Pharmaceuticals Inc (2002):
- "Product Information. Claforan (cefotaxime)." Hoechst Marion Roussel (2002):
- "Product Information. Cefotan (cefotetan)." Stuart Pharmaceuticals (2002):
Show all 19 sourcesShow fewer sources
- "Product Information. Mefoxin (cefoxitin)." Merck & Co., Inc (2002):
- "Product Information. Cefzil (cefprozil)." Bristol-Myers Squibb (2002):
- "Product Information. Fortaz (ceftazidime)." Glaxo Wellcome (2002):
- "Product Information. Cefizox (ceftizoxime)." Fujisawa (2002):
- "Product Information. Keflex (cephalexin)." Dista Products Company (2002):
- "Product Information. Cedax (ceftibuten)." Schering-Plough (2001):
- "Product Information. Maxipime (cefepime)." Bristol-Myers Squibb (2001):
- "Product Information. Omnicef (cefdinir)." Parke-Davis (2001):
- "Product Information. Ceclor CD (cefaclor)." Dura Pharmaceuticals (2001):
- "Product Information. Spectracef (cefditoren)." TAP Pharmaceuticals Inc (2001):
- "Product Information. Fetroja (cefiderocol)." Shionogi USA Inc (2019):
Gallbladder Diseases
ModerateCeftriaxone can precipitate in the gallbladder. Sonographic abnormalities and symptoms of gallbladder disease have been reported. Therapy with ceftriaxone should be administered cautiously in patients with preexisting disease of the gallbladder, biliary tract, or liver. Serial abdominal ultrasonography may be appropriate during therapy. The drug should be discontinued in patients who develop signs and symptoms suggestive of gallbladder disease while being treated with ceftriaxone.
7 sources
- Meyboom RH, Kuiper H, Jansen A "Ceftriaxone and reversible cholelithiasis." BMJ 297 (1988): 858
- Pigrau C, Pahissa A, Gropper S, Sureda D, Martinez Vazquez JM "Ceftriaxone-associated biliary pseudolithiasis in adults." Lancet 2 (1989): 165
- Zinberg J, Chernaik R, Coman E, Rosenblatt R, brandt LJ "Reversible symptomatic biliary obstruction associated with ceftriaxone pseudolithiasis." Am J Gastroenterol 86 (1991): 1251-4
- Kirejczyk WM, Crowe HM, Mackay IM, Quintiliani R, Cronin EB "Disappearing "gallstones": biliary pseudolithiasis complicating ceftriaxone therapy." Am J Roentgenol 159 (1992): 329-30
- Lopez AJ, O'Keefe P, Morrissey M, Pickleman J "Ceftriaxone-induced cholelithiasis." Ann Intern Med 115 (1991): 712-4
- "Product Information. Rocephin (ceftriaxone)." Roche Laboratories (2002):
- Maranan MC, Gerber SI, Miller GG "Gallstone pancreatitis caused by ceftriaxone." Pediat Inf Dis J 17 (1998): 662-3
Liver Diseases
ModerateCeftriaxone is eliminated by both renal and hepatobiliary excretion. At usual dosages (i.e. 1 to 2 g/day), adjustments are generally not necessary in either renal or hepatobiliary impairment. However, serum drug concentrations should be monitored periodically, and the dosage decreased accordingly if drug accumulation occurs. In patients with both hepatic and severe renal impairment, ceftriaxone dosage should not exceed 2 grams per day without close monitoring of serum concentrations.
15 sources
- Stoeckel K, Koup JR "Pharmacokinetics of ceftriaxone in patients with renal and liver insufficiency and correlations with a physiologic nonlinear protein binding model." Am J Med 77 (1984): 26-32
- Pollock AA, Tee PE, Patel IH, Spicehandler J, Simberkoff MS, Rahal JJ "Pharmacokinetic characteristics of intravenous ceftriaxone in normal adults." Antimicrob Agents Chemother 22 (1982): 816-23
- McNamara PJ, Stoeckel K, Ziegler WH "Pharmacokinetics of ceftriaxone following intravenous administration of a 3g dose." Eur J Clin Pharmacol 22 (1982): 71-5
- Wise R, Wright N "The pharmacokinetics of cefotaxime and ceftriaxone in renal and hepatic dysfunction." Infection 13 (1985): s145-50
- Fraschini F, Braga PC, Scarpazza G, et al. "Human pharmacokinetics and distribution in various tissues of ceftriaxone." Chemotherapy 32 (1986): 192-9
- Holazo, AA, Patel IH, Weinfeld RE, Konikoff JJ, Parsonnet M "Ceftriaxone pharmacokinetics following multiple intramuscular dosing." Eur J Clin Pharmacol 30 (1986): 109-12
- Garcia RL, Santivanez V, Battilana CA "Single-dose pharmacokinetics of ceftriaxone in patients with end-stage renal disease and hemodialysis." Chemotherapy 34 (1988): 261-6
- Hary L, Andrejak M, Leleu S, et al. "The pharmacokinetics of ceftriaxone and cefotaxime in cirrhotic patients with ascites." Eur J Clin Pharmacol 36 (1989): 613-6
Show all 15 sourcesShow fewer sources
- Patel IH, Chen S, Parsonnet M, et al. "Pharmacokinetics of ceftriaxone in humans." Antimicrob Agents Chemother 20 (1981): 634-41
- Stoeckel K, Tuerk H, Trueb V, McNamara PJ "Single-dose ceftriaxone kinetics in liver insufficiency." Clin Pharmacol Ther 36 (1984): 500-9
- Stoeckel K, McNamara PJ, Hoppe-Seyler G, Blumberg A, Keller E "Single-dose ceftriaxone kinetics in functionally anephric patients." Clin Pharmacol Ther 33 (1983): 633-41
- Ti TY, Fortin L, Kreeft JH, East DS, Ogilvie RI, Somerville PJ "Kinetic disposition of intravenous ceftriaxone in normal subjects and patients with renal failure on hemodialysis or peritoneal dialysis." Antimicrob Agents Chemother 25 (1984): 83-7
- Kowalsky SF, Echols RM, Parker MA "Pharmacokinetics of ceftriaxone in subjects with renal insufficiency." Clin Pharm 4 (1985): 177-81
- Cohen D, Appel GB, Scully B, Neu HC "Pharmacokinetics of ceftriaxone in patients with renal failure and in those undergoing hemodialysis." Antimicrob Agents Chemother 24 (1983): 529-32
- "Product Information. Rocephin (ceftriaxone)." Roche Laboratories (2002):
Liver Diseases
ModerateCases of hepatitis have been reported with the use of certain cephalosporins. Transient rise in AST, ALT, and alkaline phosphatase levels have also been observed. Caution and monitoring is recommended when these agents are prescribed to patients with hepatic disorders.
20 sources
- "Product Information. Vantin (cefpodoxime)." Pharmacia and Upjohn
- "Product Information. Ceclor (cefaclor)." Lilly, Eli and Company (2002):
- "Product Information. Duricef (cefadroxil)." Bristol-Myers Squibb (2002):
- "Product Information. Ancef (cefazolin)." SmithKline Beecham (2002):
- "Product Information. Kefzol (cefazolin)." Lilly, Eli and Company (2002):
- "Product Information. Suprax (cefixime)." Lupin Pharmaceuticals Inc (2002):
- "Product Information. Claforan (cefotaxime)." Hoechst Marion Roussel (2002):
- "Product Information. Cefotan (cefotetan)." Stuart Pharmaceuticals (2002):
Show all 20 sourcesShow fewer sources
- "Product Information. Mefoxin (cefoxitin)." Merck & Co., Inc (2002):
- "Product Information. Cefzil (cefprozil)." Bristol-Myers Squibb (2002):
- "Product Information. Fortaz (ceftazidime)." Glaxo Wellcome (2002):
- "Product Information. Cefizox (ceftizoxime)." Fujisawa (2002):
- "Product Information. Ceftin (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Zinacef (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Keflex (cephalexin)." Dista Products Company (2002):
- "Product Information. Cedax (ceftibuten)." Schering-Plough (2001):
- "Product Information. Maxipime (cefepime)." Bristol-Myers Squibb (2001):
- "Product Information. Omnicef (cefdinir)." Parke-Davis (2001):
- "Product Information. Ceclor CD (cefaclor)." Dura Pharmaceuticals (2001):
- "Product Information. Spectracef (cefditoren)." TAP Pharmaceuticals Inc (2001):
Pancreatitis
ModerateCases of pancreatitis, possibly secondary to biliary obstruction, have been reported rarely in patients treated with ceftriaxone. Most patients presented with risk factors for biliary stasis and biliary sludge (preceding major therapy, severe illness, total parenteral nutrition). A cofactor role of ceftriaxone-related biliary precipitation cannot be ruled out.
1 source
- "Product Information. Rocephin (ceftriaxone)." Roche Laboratories (2002):
Vitamin K Deficiency
ModerateAlterations in prothrombin times have rarely occurred in patients treated with ceftriaxone. Patients with impaired vitamin K synthesis or low vitamin K stores, such a patients with chronic hepatic disease and malnutrition, require monitoring of prothrombin time during treatment. Vitamin K administration (10 mg per week) might be needed if prothrombin time is prolonged before or during therapy.
1 source
- "Product Information. Rocephin (ceftriaxone)." Roche Laboratories (2002):