Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ceftazidime
Drug ID BADD_D00399
Description Bacteria possess a cell wall comprising a glycopeptide polymer commonly known as peptidoglycan, which is synthesized and remodelled through the action of a family of enzymes known as "penicillin-binding proteins" (PBPs).[A232920] β-lactam antibiotics, including cephalosporins, are PBP inhibitors that, through inhibition of essential PBPs, result in impaired cell wall homeostasis, loss of cell integrity, and ultimately bacterial cell death.[A232920, A232925, A232930] Ceftazidime is a third-generation cephalosporin with broad-spectrum antibacterial activity, including against some treatment-resistant bacteria such as _Pseudomonas aeruginosa_.[L32935] Ceftazidime was approved by the FDA on July 19, 1985, and is currently available either alone or in combination with the non-β-lactam β-lactamase inhibitor [avibactam] to treat a variety of bacterial infections.[L32935, L32940]
Indications and Usage Ceftazidime is indicated for the treatment of lower respiratory tract infections, skin and skin structure infections, urinary tract infections, bacterial septicemia, bone and joint infections, gynecologic infections, intra-abdominal infections (including peritonitis), and central nervous system infections (including meningitis) caused by susceptible bacteria.[L32935] Ceftazidime is indicated in combination with [avibactam] to treat infections caused by susceptible Gram-negative organisms, including complicated intra-abdominal infections (cIAI), in conjunction with [metronidazole], and complicated urinary tract infections (cUTI), including pyelonephritis, in patients aged three months and older. This combination is also indicated to treat hospital-acquired and ventilator-associated bacterial pneumonia (HABP/VABP) in patients aged 18 years and older.[L32940] In all cases, to mitigate the risk of bacterial resistance and preserve clinical efficacy, ceftazidime should only be used for infections that are confirmed or strongly suspected to be caused by susceptible bacterial strains.[L32935, L32940]
Marketing Status approved
ATC Code J01DD02
DrugBank ID DB00438
KEGG ID D00921; D07654
MeSH ID D002442
PubChem ID 5481173
TTD Drug ID D0PH5Z
NDC Product Code 0264-3145; 25021-127; 0409-5082; 10402-013; 0409-5084; 0409-5086; 0409-5092; 82608-010; 0409-5093; 25021-128; 44567-235; 0264-3143; 52946-0924; 44567-237; 25021-129; 44567-236
UNII 9M416Z9QNR
Synonyms Ceftazidime | Fortaz | Fortum | Ceftazidime Pentahydrate | LY-139381 | LY 139381 | LY139381 | Tazidime | Ceftazidime Anhydrous | Pyridinium, 1-((7-(((2-amino-4-thiazolyl)((1-carboxy-1-methylethoxy)imino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-, inner salt, pentahydrate, (6R-(6alpha,7beta(Z)))- | GR-20263 | GR 20263 | GR20263
Chemical Information
Molecular Formula C22H22N6O7S2
CAS Registry Number 72558-82-8
SMILES CC(C)(C(=O)O)ON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)C[N+]4=CC=CC=C4)C(=O)[O -]
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Hyperbilirubinaemia01.06.04.003; 14.11.01.010; 09.01.01.003--Not Available
Hypercapnia22.02.02.002; 14.01.04.0010.000073%Not Available
Hyperhidrosis23.02.03.004; 08.01.03.0280.000049%
Hypersensitivity10.01.03.0030.000097%
Hypotension24.06.03.0020.000170%
Hypothermia12.05.03.001; 08.05.01.0030.000073%
Hypoventilation22.02.01.0070.000073%Not Available
Immune system disorder10.02.01.001--Not Available
Impaired gastric emptying07.02.02.0040.000073%
Injection site pain12.07.03.011; 08.02.03.010--Not Available
Jaundice23.03.03.030; 09.01.01.004; 01.06.04.004--Not Available
Lethargy19.04.04.004; 17.02.04.003; 08.01.01.008--
Leukopenia01.02.02.001--Not Available
Local reaction08.01.03.012--Not Available
Loss of consciousness17.02.04.0040.000049%Not Available
Lymphocytosis01.02.01.003--Not Available
Mania19.16.02.0020.000097%
Menopausal symptoms21.02.02.002--Not Available
Mouth ulceration07.05.06.0040.000049%Not Available
Myoclonus17.02.05.008--Not Available
Nausea07.01.07.001--
Nephropathy toxic20.05.03.002; 12.03.01.010--Not Available
Nervous system disorder17.02.10.0010.000049%Not Available
Neutropenia01.02.03.0040.000097%Not Available
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.0070.000073%
Oral candidiasis11.03.03.004; 07.05.07.001--Not Available
Pain08.01.08.004--
Pancytopenia01.03.03.003--Not Available
Paraesthesia23.03.03.094; 17.02.06.0050.000073%
Phlebitis24.12.03.004; 12.02.01.002--
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ADReCS-Target
Drug Name ADR Term Target
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