Drug Database
PI

piperacillin (piperacillin, KRKA / Isipen)

✓ Approved

Krka · Small Molecule · Small Molecule

What is piperacillin?

piperacillin is a small molecule developed by Krka. It is approved for therapeutic indications via unknown.

Drug Profile

Brand Namespiperacillin, KRKA, Isipen
CompanyKrka
Drug ClassSmall Molecule
RouteUnknown
StatusApproved

Therapeutic Indications

piperacillin is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Infections and infestationsSalmonellosis✓ Approved

Related Research Articles

PubMedHCA healthcare journal of medicine2026-07-25

Autoimmune Hemolytic Anemia Associated With Leptospirosis: A Rare Complication.

Waqar Anum A, Mazhar Furqan F, Afzal Mahrukh M, Razzaq Sadia S et al.

Autoimmune hemolytic anemia (AIHA) is rare but potentially life-threatening complication of leptospirosis, a zoonotic infection caused by the Leptospira species. Autoimmune hemolytic anemia occurs when the immune system targets red blood cells, resulting in hemolysis and anemia. The relationship between leptospirosis and AIHA is uncommon and often under-recognized, which can delay diagnosis and management. This case highlights the importance of considering hematologic complications in leptospirosis. A 23-year-old male presented with low-grade fever, productive cough, shortness of breath, jaundice, and pallor for 15 days. On examination, he was pale and icteric with bilateral chest crepitations. Laboratory studies showed severe anemia (hemoglobin 5.5 g/dL), elevated lactate dehydrogenase (1027 U/L), hyperbilirubinemia, thrombocytopenia, and peripheral smear evidence of hemolysis. A direct Coombs' test was strongly positive. Leptospira immunoglobulin M serology confirmed the diagnosis. The patient was managed with broad-spectrum antibiotics (piperacillin-tazobactam and doxycycline) and high-dose corticosteroids (1 mg/kg/day). He improved clinically with stabilization of hemoglobin and a resolution of symptoms. This case demonstrates a rare immune-mediated manifestation of leptospirosis presenting as AIHA without hepatic or renal failure. Clinicians should maintain a high index of suspicion for hematologic complications in leptospirosis. Early recognition and timely initiation of corticosteroid therapy alongside antibiotics can improve patient outcomes.

PubMedInternational ophthalmology2026-07-25

Antimicrobial resistance in post-cataract endophthalmitis: a systematic review on resistance pattern and treatment outcomes.

Yan Martin Chi Kit MCK, Rees Amelia A, Saleki Mohammad M

To systematically review the microbiological spectrum, antimicrobial resistance (AMR) patterns, management strategies, and outcomes in culture-positive endophthalmitis, a rare vision-threatening complication of cataract surgery increasingly challenged by resistance. A comprehensive literature search was conducted in PubMed, Embase, Scopus, and the Cochrane Central Register of Controlled Trials from 1 January 1990 to 30 June 2025. Eligible studies included culture-positive cases of acute Post-Cataract Endophthalmitis reporting antimicrobial susceptibility and outcomes. Data were extracted on organisms, resistance profiles, treatment strategies and visual acuity. Risk of bias was assessed using the ROBINS-I tool. Six studies (five retrospective, one prospective) from Europe, Asia, and North America met inclusion criteria. Coagulase-negative staphylococci predominated, with frequent methicillin and fluoroquinolone resistance; Staphylococcus, Streptococcus, and Pseudomonas were less common. An Indian cohort described multidrug-resistant Pseudomonas with near-universal resistance to fluoroquinolones, aminoglycosides, and cephalosporins but susceptibility to colistin, piperacillin, and imipenem. While vancomycin remained active against Gram-positive organisms, emerging resistance was reported in the United Kingdom. Visual outcomes varied: tap-and-inject was comparable to early pars plana vitrectomy (PPV), except in Gram-negative infections where PPV conferred benefit. Amikacin resistance correlated with poorer outcomes, whereas vancomycin or moxifloxacin resistance did not. Systemic antibiotics and intravitreal corticosteroids showed no consistent benefit. AMR in Post-Cataract Endophthalmitis is an escalating concern with marked geographic variation. Prompt intravitreal therapy remains the key determinant of prognosis, but empiric regimens must reflect local resistance trends, particularly for Gram-negative coverage. Current evidence is limited by retrospective design and regional variability; multicentre prospective studies are needed to refine prophylaxis and treatment protocols, reducing visual and economic burden.

PubMedInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2026-07-25

Global genomic surveillance of β-lactam resistance in Escherichia coli across human, animal, and environmental reservoirs.

Sholeh Mohammad M, Beig Masoumeh M, Kiani Negin N, Badmasti Farzad F

Escherichia coli poses a global health threat from increasing β-lactam resistance. This study uses genomic and One-Health data to map resistance patterns and enhance antimicrobial resistance (AMR) prediction and management. This study performed a One-Health whole-genome analysis of 30,554 E. coli isolates from human, animal, and environmental sources, spanning from 2000 to 2025. Publicly available genomic data were retrieved from NCBI, encompassing β-lactam resistance genes, including extended-spectrum β-lactamases, AmpC, and carbapenemases, along with key chromosomal resistance modifiers. These genes were identified and curated using AMRFinderPlus. Multilocus sequence typing (MLST) and pathotype assignments were conducted in silico. Temporal, host, sequence-type (ST), and geographic patterns of resistance were modeled, with gradient-boosted machine learning algorithms predicting minimum inhibitory concentrations (MICs) based on antibiotic resistance gene profiles and chromosomal features. Temporal and geographic resistance patterns were further analyzed using statistical and visualization tools in R and Python. A total of 30,554 E. coli whole-genome sequences from isolates spanning 126 countries between 2000 and 2025 were analyzed. The dataset included 2015 complete genomes, 177 chromosome-level assemblies, 8310 scaffold-level assemblies, and 20,052 contig-level assemblies, with an average sequence length of 5,120,983 bp. Isolates were categorized by host source: 14,320 from humans, 8184 from animals, 3941 from environmental sources, and 4109 with an unknown source. MLST was successfully performed on 29,648 isolates, identifying dominant STs such as ST131, ST11, and ST10. Human isolates were predominantly associated with epidemic clones ST131, ST73, and ST1193, while animal isolates were associated with ST10, and environmental isolates showed a strong presence of ST155. Temporal analyses indicated a steady increase in β-lactam resistance, with blaCTX-M-15, blaNDM-5, and blaOXA-1 showing the most significant prevalence trends. Model performance was strongest for carbapenems, particularly imipenem (R2 = 0.88) and ertapenem (R2 = 0.74), whereas predictions for ampicillin and piperacillin-tazobactam showed poor agreement with observed MICs. Global analysis of 30,554 genomes shows rising β-lactam resistance driven by key genes (blaCTX-M-15, blaNDM-5, blaOXA-1) in high-risk clones. Machine learning accurately predicted carbapenem resistance but struggled with β-lactamase inhibitor combos. Integrating genomics and One-Health data can guide AMR surveillance and control.

PubMedInternational journal of clinical pharmacy2026-07-24

Active surveillance and risk prediction of piperacillin/tazobactam‑associated hypokalaemia: development and external validation of a clinical nomogram.

Bai Hehe H, Guo Miao M, Zheng Nanbo N, Nie Xiaojing X

Piperacillin/tazobactam (TZP) is widely used in hospitalised adults. Real‑world data suggest a higher risk of hypokalaemia than previously recognised. To investigate incidence, severity and risk factors of TZP‑induced hypokalaemia, and to develop and externally validate a nomogram for individualised risk prediction. This retrospective study included hospitalised adults receiving TZP (2021-2025). TZP‑induced hypokalaemia was defined as serum potassium < 3.5 mmol/L ≥ 48 h after TZP initiation. Logistic regression identified predictors. A nomogram was constructed. Model performance was assessed by discrimination (area under the ROC curve, AUC), calibration (Hosmer‑Lemeshow test, calibration intercept/slope), Brier score and decision‑curve analysis (DCA), with internal and external validation. Among 643 patients, 122 (19.0%) developed TZP‑induced hypokalaemia (mild: 78.7%; moderate: 16.4%; severe: 4.9%). Median time to onset was 5.0 days. Independent predictors were age ≥ 65 years (OR = 2.118, 95% CI 1.003-4.472, p = 0.049), body mass index (OR = 0.671, 95% CI 0.591-0.762, p < 0.001), intensive care unit admission (OR = 2.915, 95% CI 1.504-5.651, p = 0.002), daily dose (OR = 1.280, 95% CI 1.110-1.476, p < 0.001), and baseline serum potassium (OR = 0.123, 95% CI 0.056-0.271, p < 0.001). The nomogram showed good discrimination (training AUC 0.881, internal 0.876, external 0.813), calibration (Hosmer‑Lemeshow p > 0.05), Brier scores < 0.25 and positive net benefit on DCA. TZP‑induced hypokalaemia is common in hospitalised adults. A nomogram based on five readily available clinical variables may facilitate early identification of high‑risk patients, although prospective validation in diverse settings is required before clinical implementation.

PubMedThe Journal of antimicrobial chemotherapy2026-07-24

Predictive performance of an antibiotic precision dosing software program in critically ill adults with infection.

Williams Paul P, Cotta Menino Osbert MO, Wilks Kathryn K, Farkas Andras A et al.

Critically ill patients exhibit altered pharmacokinetics, rendering antibiotic dosing challenging. Achieving therapeutic antibiotic exposures may be improved with the use of precision dosing software programs. To quantify and compare both a priori and a posteriori predictive performance of an antibiotic precision dosing software program in a heterogenous cohort of critically ill adults with infection. The precision dosing program, ID-ODSTM, was used to predict a priori and a posteriori concentrations for piperacillin, meropenem, cefepime, flucloxacillin and vancomycin using clinical and demographic data derived from a previous study in critically ill adults (GUIDE trial). Predicted concentrations were compared to observed concentrations using pre-specified acceptance criteria (median predictive error (MDPE) ≤20% and median absolute predictive error (MDAPE) ≤30%), along with F20 and F30 metrics. Furthermore, the impact of predictions on theoretical dosing recommendations to achieve pre-defined drug exposures was assessed. The a priori predictive performance in 81 patients administered beta-lactams did not meet any pre-specified acceptance criteria (pooled MDPE -35% and MDAPE 58%). However, all beta-lactams met accuracy acceptance criteria for the a posteriori approach (pooled MDPE -3.6%), although only cefepime demonstrated acceptable precision and F20 and F30 acceptance. In 25 patients administered vancomycin, a priori predictive performance met all acceptance criteria for accuracy and precision.When assessing a priori theoretical dosing recommendation concordance, approximately one in three predictions led to an unnecessary dosing action. Concordance was similar with an a posteriori approach, however, overprediction was observed in 20% of meropenem predictions. In a heterogenous adult ICU population, the a priori predictive performance of vancomycin was shown to be acceptable. Conversely, the a priori predictive performance for the beta-lactams was not acceptable. Although predictive performance improved with the a posteriori approach for beta-lactams, only cefepime met acceptance criteria.

PubMedReports (MDPI)2026-07-24

A Minor Sports Injury with Major Consequences: Probable Streptococcal Toxic Shock Syndrome and Necrotizing Soft Tissue Infection in a Young Adult-A Case Report.

Stangiewicz Bartosz B, Korzep Lukasz L

Background and Clinical Significance:Streptococcus pyogenes (group A Streptococcus, GAS) can cause rapidly progressive invasive infections, including necrotizing soft tissue infection (NSTI) and streptococcal toxic shock syndrome (STSS). Although invasive GAS disease is often associated with skin barrier disruption, severe infection may also follow blunt trauma without visible skin injury. Case Presentation: A 22-year-old woman presented with persistent right hip and groin pain four days after a blunt fall during recreational sports activity, without disruption of skin integrity. On admission, she was hypotensive, tachycardic, and intermittently hypoxemic, with local hematoma, swelling, and inflammatory infiltration of the right groin. Laboratory tests showed marked inflammation, acidosis, acute kidney injury (AKI), elevated lactate, creatine kinase, and myoglobin levels. She was admitted to the intensive care unit with septic shock. Empirical antimicrobial therapy was initiated with piperacillin/tazobactam, clindamycin, and linezolid. Computed tomography showed inflammatory changes extending from the right groin to the thigh fascia. On day 3, the patient's condition deteriorated with respiratory failure necessitating endotracheal intubation and mechanical ventilation. Surgical incision revealed inflamed and necrotic subcutaneous tissue with superficial muscle involvement. Deep tissue cultures yielded GAS, whereas blood and urine cultures remained negative; probable STSS was diagnosed. Therapy was de-escalated to penicillin plus clindamycin. Continuous renal replacement therapy with an adsorptive acrylonitrile 69 surface-treated (AN69ST) membrane was initiated for AKI. The patient gradually improved and was transferred to the surgical ward on day 16. Conclusions: Minor blunt trauma without skin disruption may precede life-threatening invasive GAS infection. Rapid recognition, surgical source control, antitoxin antimicrobial therapy, and intensive organ support are essential in suspected STSS.

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