| Fact Table | |
|---|---|
| Formula | C40H66N2O12 / (C18H31NO4)2·C4H4O4 (bisoprolol fumarate); C7H8ClN3O4S2 (hydrochlorothiazide) |
| License | FDA approved (Ziac NDA 020186; U.S. prescription product; generic equivalents available) |
| Bioavailability | Both components are well absorbed after oral Ziac; no change in bioavailability when combined. Bisoprolol absolute bioavailability ~80%; hydrochlorothiazide oral absorption ~65–75% |
| Legal status | Prescription only (Rx only) |
| Chemical Name | Bisoprolol fumarate: (±)-1-[4-[[2-(1-methylethoxy)ethoxy]methyl]phenoxy]-3-[(1-methylethyl)amino]-2-propanol (E)-2-butenedioate (2:1) salt; Hydrochlorothiazide: 6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide |
| Elimination half-life | In Ziac studies: bisoprolol ~7–15 hours; hydrochlorothiazide ~4–10 hours. Individually reported: bisoprolol ~9–12 hours; hydrochlorothiazide ~6–15 hours |
| Dosage (Strength) | Film-coated oral tablets: 2.5 mg/6.25 mg, 5 mg/6.25 mg and 10 mg/6.25 mg bisoprolol fumarate/hydrochlorothiazide; usual initial dose 2.5 mg/6.25 mg once daily; titrate every 14 days up to maximum 20 mg/12.5 mg once daily |
| Pregnancy | No adequate well-controlled studies in pregnant women; use only if potential benefit justifies fetal risk. Thiazides cross the placenta and may cause fetal/neonatal jaundice, thrombocytopenia or other adverse reactions |
| Brands | Ziac; generic bisoprolol fumarate/hydrochlorothiazide tablets; related international brands include Lodoz and Bilocor Plus |
| Protein binding | Bisoprolol approximately 30%; hydrochlorothiazide approximately 40–68% |
| PubChem CID | 44153906 (bisoprolol fumarate/hydrochlorothiazide combination); 5281064 (bisoprolol fumarate); 2405 (bisoprolol); 3639 (hydrochlorothiazide) |
| MedlinePlus | a693024 (bisoprolol); a682571 (hydrochlorothiazide); Ziac cross-referenced to both component monographs |
| ChEBI | 3127 (bisoprolol); 5778 (hydrochlorothiazide) |
| ATC code | C07BB07 |
| DrugBank | DB00612 (bisoprolol); DB00999 (hydrochlorothiazide); DBSALT001015 (bisoprolol fumarate) |
| KEGG | D10275 (bisoprolol fumarate and hydrochlorothiazide); D02342 (bisoprolol fumarate); D00340 (hydrochlorothiazide) |
| Routes of administration | By mouth (oral film-coated tablets) |
Zirgan (ganciclovir ophthalmic gel 0.15%) is a prescription eye medicine used to treat a herpes infection of the cornea, the clear front part of the eye. This infection can cause dendritic (branching) ulcers on the cornea. Zirgan helps stop the herpes virus from making more copies of itself, which helps the eye heal. It comes as a sterile, clear gel that is placed directly in the affected eye. It is approved for adults and children 2 years and older.
Zirgan is only for use in the eye.
Put 1 drop in the affected eye 5 times a day, about every 3 hours while awake, until the corneal ulcer heals.
After it heals, use 1 drop in the affected eye 3 times per day for 7 more days.
Tilt your head back, gently pull down your lower eyelid, and place 1 drop in the small pocket without touching the tube tip to your eye, eyelid, fingers, or any surface.
Close your eye gently for a moment, then recap the tube immediately.
Wash your hands before and after using Zirgan.
Keep all follow-up visits with your eye care provider so they can check how it heals.
The active ingredient in Zirgan is ganciclovir. The inactive ingredients may include carbomer homopolymer, water for injection, sodium hydroxide, and mannitol. The gel is preserved with benzalkonium chloride.
Before using this medication, you may want to consult a healthcare provider about the following:
Do not swallow Zirgan or apply it to other parts of the body.
Do not wear contact lenses if you have any signs or symptoms of herpetic keratitis or while you are using Zirgan. Contact lenses can trap viruses and medication against the eye and worsen the infection.
Avoid touching the tip of the tube to your eye, eyelid, fingers, or any other surface. This can contaminate the gel and lead to a new eye infection. Recap the tube right after each use.
Tell your healthcare provider if eye pain develops or if redness, itching, or inflammation gets worse while using Zirgan. These can be signs of irritation, an allergic reaction, or a new infection.
Blurred vision can happen right after applying Zirgan. Do not drive or use machinery until your vision has improved.
Use during pregnancy should be guided by a healthcare provider. There is no human data on the use of topical ganciclovir during pregnancy, and animal studies with intravenous ganciclovir have shown harm to an unborn baby.
Caution should be used when Zirgan is given to nursing mothers. It is not known whether topical ganciclovir passes into human breast milk.
Animal data suggest that systemic (intravenous) ganciclovir at high doses may affect fertility in both males and females. Whether topical use in the eye causes enough absorption into the body to reduce fertility in humans is unknown.
Zirgan should not be used in children under 2 years of age.
There are no contraindications for Zirgan listed in the prescribing information.
Common side effects of Zirgan include:
Stop using Zirgan and seek medical attention if you have signs of a serious allergic reaction, such as swelling of the face, lips, tongue, or throat, trouble breathing, severe rash, or hives.
Contact your eye care provider if redness, itching, vision, or inflammation gets worse, or if the corneal ulcer is not healing as expected.
Any signs of a possible new eye infection, such as discharge, increased pain, or sensitivity to light, should also be evaluated.
A generic drug is a copy of the brand-name drug with the same dosage, safety, strength, quality, consumption method, performance, and intended use. Before generics become available on the market, the generic company must prove it has the same active ingredients as the brand-name drug and works in the same way and in the same amount of time in the body.
The only differences between generics and their brand-name counterparts is that generics are less expensive and may look slightly different (e.g., different shape or color), as trademark laws prevent a generic from looking exactly like the brand-name drug.
Generics are less expensive because generic manufacturers don't have to invest large sums of money to develop a drug. When the brand-name patent expires, generic companies can manufacture a copy of the brand-name and sell it at a substantial discount.