hyperemia

Among netarsudil-treated patients, the most frequent ocular adverse event was conjunctival hyperemia (47.9 percent), which was mostly mild.

In clinical trials of Rhopressa, the most common adverse reactions were conjunctival hyperemia, corneal verticillata, instillation site pain, and conjunctival hemorrhage.

The most common ocular adverse reactions in subjects treated with Dextenza were: anterior chamber inflammation including iritis and iridocyclitis, increased intraocular pressure, reduced visual acuity, cystoid macular edema, corneal edema, eye pain, and conjunctival hyperemia. The most common non-ocular adverse event was headache.

Marginal hyperemia of the pectoral and pelvic fins; increased beating of the spiracle; variation in motor activity with hyperexcitation phase; and contraction in the gill region, for expulsion of water through the spiracles.

The most common OP0201 adverse events occurring in more than 2 participants and greater than placebo were tympanic membrane hyperemia and tympanic membrane disorder.

On physical examination, increase in the diameter and temperature, hyperemia, and tenderness were detected in the right leg.

The symptoms (itching, photophobia, lacrimation, pain) and signs (conjunctival hyperemia /chemosis, size of giant papillae, limbal infiltrate, shield ulcers/keratitis and trantas dots were recorded.

Due to the inflammation, orbital signs and symptoms, such as pain, proptosis, ptosis, periorbital pain, diplopia, ophthalmoplegia, conjunctival hyperemia or ocular injection can be seen (8).

Such criteria were; alveolar generation, thickening in interalveolar septum, capillary hyperemia, hemorrhage, inflammatory cell infiltration, terminal bronchiole structure, terminal bronchiole debris, respiratory bronchiole wall structure, respiratory wall debris, alveolar structure and edema in vascular wall.

Significant improvement in VAS, SF-36, WOMAC score, hyperemia, and thickness of suprapatellar recess synovium from baseline was seen up to 6 months after intra-articular HA injection.

The patients were put on cyclosporine 0.1% eyedrops two times a day after stopping their previous medication and then evaluated for the symptoms (Itching, discharge, photophobia and watering) and signs (Conjunctival hyperemia, papillary hypertrophy, Horner Trantas spots and punctata keratitis) and subsequently graded as described below at baseline, on 2nd week, 4th week, and 12th week.

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