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Each register with its number of medicines and a few of them.
Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.
AEMPS · 11 medicines
Health Canada · 10 medicines
FDA · 10 medicines
AIFA · 8 medicines
SFDA · 8 medicines · Historical list
HSA · 7 medicines
MS · 6 medicines · Historical list
ALIMS · 4 medicines
TFDA · 4 medicines
HALMED · 2 medicines
PHARMAC · 2 medicines
EMA · 1 medicine
Every register, a page at a time. Strengths and packs are on each medicine’s page.
10 results
| Medicine | Register | Strength | Form | Status | Holder |
|---|---|---|---|---|---|
| Granisetron Hydrochloride | United States | 1MG BASE | tablet | Marketed | Barr |
| Granisetron Hydrochloride | United States | 2MG BASE/10ML | solution | Marketed | Intra Sana Labs |
| Granisetron Hydrochloride | United States | 0.1MG BASE/ML, 1MG BASE/ML, 1MG/ML … | injectable | Marketed | Fresenius Kabi USA |
| Granisetron Hydrochloride Preservative Free | United States | 1MG BASE/ML | injectable | Marketed | DR Reddys |
| Granisol | United States | 2MG BASE/10ML | solution | Not marketed | Intra Sana Labs |
| Sancuso | United States | 3.1MG/24HR | film, extended release | Marketed | Cumberland |
| Sustol | United States | 10MG/0.4ML | injectable | Marketed | Heron Theraps INC |
| Kytril | United States | 2MG BASE/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | solution | Not marketed | Roche |
| Kytril | United States | 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for sa | injectable | Not marketed | Roche |
| Kytril | United States | 1MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons**, 2MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons** | tablet | Not marketed | Roche |
The same brand on several registers.
The companies holding its medicines, the most first.
How the registers write it, in their own languages.
Compiled by Prognia from the public medicine registers of AEMPS, AIFA, ALIMS, Anvisa, CBG-MEB, EMA, FDA, HALMED, Health Canada, HSA, MS, PHARMAC, SFDA and TFDA. Each medicine’s page names its own source, licence and attribution.
Report an error or request removalCorrections from a register or a company are welcome.
For reference and learning, not treatment advice. Always check the official product information.
