ondansetron has been researched along with amifostine anhydrous in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Benz, RD; Contrera, JF; Kruhlak, NL; Matthews, EJ; Weaver, JL | 1 |
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
Gallegos-Castorena, S; Guerrero-Avendaño, G; Martínez-Avalos, A; Medina-Sansón, A; Mohar-Betancourt, A; Zapata-Tarrés, M | 1 |
1 review(s) available for ondansetron and amifostine anhydrous
Article | Year |
---|---|
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk | 2016 |
1 trial(s) available for ondansetron and amifostine anhydrous
Article | Year |
---|---|
Toxicity prevention with amifostine in pediatric osteosarcoma patients treated with cisplatin and doxorubicin.
Topics: Adolescent; Amifostine; Antiemetics; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Calcium Gluconate; Child; Cisplatin; Doxorubicin; Female; Hearing Loss; Heart Diseases; Humans; Hypocalcemia; Infusions, Intra-Arterial; Infusions, Intravenous; Kidney Diseases; Male; Neoadjuvant Therapy; Ondansetron; Osteosarcoma; Prospective Studies; Severity of Illness Index; Treatment Outcome; Vomiting | 2007 |
1 other study(ies) available for ondansetron and amifostine anhydrous
Article | Year |
---|---|
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
Topics: Adverse Drug Reaction Reporting Systems; Artificial Intelligence; Computers; Databases, Factual; Drug Prescriptions; Drug-Related Side Effects and Adverse Reactions; Endpoint Determination; Models, Molecular; Quantitative Structure-Activity Relationship; Software; United States; United States Food and Drug Administration | 2004 |