A Randomized Double-Masked Trial Comparing Ketorolac Tromethamine 0.5%, Diclofenac Sodium 0.1%, and Prednisolone Acetate 1% in Reducing Post-Phacoemulsification Flare and Cells

1998 ◽  
Vol 29 (7) ◽  
pp. 539-544
Author(s):  
Sherif M El-Harazi ◽  
Richard S Ruiz ◽  
Robert M Feldman ◽  
Guillermina Villanueva ◽  
Alice Z Chuang
1997 ◽  
Vol 7 (3) ◽  
pp. 236-240 ◽  
Author(s):  
T.A. Demco ◽  
H. Sutton ◽  
C.J. Demco ◽  
P. Sunder Raj

Purpose. This study was performed to compare the efficacy, safety and tolerability of diclofenac sodium 0.1 % ophthalmic solution with that of prednisolone acetate 1.0% ophthalmic suspension for treatment of inflammation following phacoemulsification and posterior chamber lens implantation. Methods. One hundred and sixteen patients (diclofenac 57, prednisolone 59) with visually disabling cataract were enrolled in this prospective, randomised, double-masked, parallel group study in two centres. Post-operative patient assessments at day 1, 5–8 and 12–16 included visual acuity, slit-lamp examination, applanation tonometry and subjective evaluation of local tolerance. Results. There was no statistically significant difference between the diclofenac and prednisolone groups in the sum of the grades of anterior chamber flare and cells or the degree of conjunctival hyperaemia at any study visit. The overall assessment of local tolerance was similar for both the study medications. There were two (3.4%) possibly drug-related adverse events in the prednisolone group but neither was severe. Conclusions. Diclofenac sodium 0.01% ophthalmic solution was as effective, safe and well tolerated overall as prednisolone acetate 1.0% ophthalmic suspension.


1999 ◽  
Vol 25 (8) ◽  
pp. 1097-1108 ◽  
Author(s):  
Marguerite B. McDonald ◽  
Stephen F. Brint ◽  
Daniel I. Caplan ◽  
Linda B. Bourque ◽  
Kimberly Shoaf

2019 ◽  
Vol 71 (6) ◽  
pp. 1865-1872 ◽  
Author(s):  
F.Q. Pereira ◽  
B. Santos ◽  
T. Carboni ◽  
M. Bender ◽  
D. Driemeier ◽  
...  

ABSTRACT The effect of the systemic absorption of 0.1% diclofenac sodium (DS) eyedrop was compared to that of 0.5% ketorolac tromethamine (KT) in female New Zealand white rabbits treated on both eyes three times a day for 90 days. The rabbits were divided in three groups of six animals (n= 18): KT group, DS group, and control (Co) group, in which saline (0.9% NaCl) solution was instilled. Water and food consumption were measured daily, clinical examination was performed weekly, and blood samples were collected every 30 days for laboratory examination. The plasma was analyzed for the presence of KT and DS by solid-phase extraction (SPE) associated with mass spectrometry (MS). Systemic absorption of these drugs was confirmed by SPE-MS, allowing their separation and identification in the plasma. At the end of the treatment, the animals were euthanized and necropsied, and no macroscopic or microscopic changes were found. This observation confirmed the laboratory results, which were within normal reference standards for the species. According to the results obtained, it can be concluded that treatment with eyedrops containing KT and DS for 90 days in healthy rabbits does not cause adverse systemic effects.


2012 ◽  
Vol 60 (4) ◽  
pp. 277 ◽  
Author(s):  
Rodrigo PessoaCavalcanti Lira ◽  
FernandoRoberte Zanetti ◽  
Carlos EduardoLeite Arieta ◽  
Fernando RodrigoPedreira Chaves ◽  
AlexandrePaashaus da Costa Pinto ◽  
...  

2017 ◽  
Vol 7 (3) ◽  
pp. 254 ◽  
Author(s):  
Raquel de Araújo Cantarella ◽  
Juliana Kravetz De Oliveira ◽  
Daniel M. Dorbandt ◽  
Fabiano Montiani-Ferreira

1994 ◽  
Vol 13 (2) ◽  
pp. 111-117 ◽  
Author(s):  
Gary J. Chellman ◽  
Lance O. Lollini ◽  
Albert E. Dorr ◽  
Linval R. DePass

The local tolerance of ketorolac tromethamine (Toradol®, Syntex) was compared with that of four other injectable nonsteroidal anti-inflammatory drugs (NSAIDs) (diclofenac sodium, piroxicam, ketoprofen, and metamizol magnesium) in the rat paw-lick/muscle irritation assay as described previously,1 All drugs were tested at concentrations approved for clinical use. After subplantar (footpad) injection, ketorolac produced virtually no pain-on-injection as assessed by the number of paw-lick/lift responses during a 15 min observation period. The other NSAIDs produced slight to moderate paw-lick/lift responses. Redness and swelling at the injection site were less severe for ketorolac than for the other NSAIDs, After intramuscular (i.m.) injection, all of the. NSAIDs produced some degree of muscle damage, as assessed histopathologically 24 h after injection. The lesions, consisting primarily of muscle degeneration, were less severe for ketorolac than for the other NSAIDs. Ketorolac and metamizol produced the smallest elevations in serum creatine kinase, as measured 2 h after i.m. dosing, not significantly different from isotonic saline. Overall, ketorolac was better tolerated in the assay than the other injectable NSAIDs, thereby suggesting the possibility of improved local tolerance on clinical use.


2019 ◽  
Vol 80 (12) ◽  
pp. 1129-1135
Author(s):  
Amy J. Rankin ◽  
Kate S. KuKanich ◽  
Thomas Schermerhorn ◽  
Nora M. Bello ◽  
Jane Ashley Huey ◽  
...  

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