quinidine has been researched along with oxytetracycline, anhydrous in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andricopulo, AD; Moda, TL; Montanari, CA | 1 |
| Lombardo, F; Obach, RS; Waters, NJ | 1 |
| Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV | 1 |
| Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
| García-Mera, X; González-Díaz, H; Prado-Prado, FJ | 1 |
| Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
| Bevan, JA; Pascual, R | 1 |
| ATRIA, NF; WADSWORTH, GL | 1 |
1 review(s) available for quinidine and oxytetracycline, 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 |
7 other study(ies) available for quinidine and oxytetracycline, anhydrous
| Article | Year |
|---|---|
Hologram QSAR model for the prediction of human oral bioavailability.
Topics: Administration, Oral; Biological Availability; Holography; Humans; Models, Biological; Models, Molecular; Molecular Structure; Pharmaceutical Preparations; Pharmacokinetics; Quantitative Structure-Activity Relationship | 2007 |
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding | 2008 |
Physicochemical determinants of human renal clearance.
Topics: Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kidney; Metabolic Clearance Rate; Molecular Weight | 2009 |
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
Topics: Antiparasitic Agents; Molecular Structure; Neural Networks, Computer; Parasitic Diseases; Quantitative Structure-Activity Relationship; Species Specificity; Thermodynamics | 2010 |
Asymmetry of consequences of drug disposition mechanisms in the wall of the rabbit aorta.
Topics: Animals; Aorta, Thoracic; Biological Transport; Desipramine; Desoxycorticosterone; Dose-Response Relationship, Drug; Estradiol; Female; Histamine; Iproniazid; Male; Muscle Contraction; Norepinephrine; Oxytetracycline; Potassium Chloride; Propiophenones; Quinidine; Rabbits; Time Factors | 1980 |
TWO YEARS EXPERIENCE WITH SHIGELLOSIS IN A HOSPITAL AND SCHOOL FOR THE MENTALLY RETARDED.
Topics: Anti-Bacterial Agents; Chloramphenicol; Communicable Disease Control; Dysentery, Bacillary; Furazolidone; Kanamycin; Mental Disorders; Morbidity; Oxytetracycline; Paromomycin; Persons with Mental Disabilities; Protein Synthesis Inhibitors; Quinidine; Shigella dysenteriae; Sulfathiazoles; Tetracycline | 1963 |