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Each register with its number of medicines and a few of them.
Anvisa · 1 medicine · Historical list
Health Canada · 1 medicine · Historical list
EMA · 1 medicine · Historical list
SFDA · 1 medicine · Historical list
Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.
FDA · 1 medicine
Every register, a page at a time. Strengths and packs are on each medicine’s page.
5 results
| Medicine | Register | Strength | Form | Status | Holder |
|---|---|---|---|---|---|
| Doribax | United States | 250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | injectable | Not marketed | Shionogi |
| Doribax | European Union | Withdrawn | Janssen-Cilag International NV | ||
| Doriprex | Brazil | Cancelled | Janssen-Cilag Farmacêutica Ltda | ||
| Doribax | Canada | 500 MG / VIAL | Powder For Solution | Cancelled | Janssen INC |
| Doribax 500MG/Vial Powder for Infusion | Saudi Arabia | Authorised | Shionogi & Co. LTD |
The same brand on several registers.
The companies holding its medicines, the most first.
Compiled by Prognia from the public medicine registers of Anvisa, EMA, FDA, Health Canada and SFDA. 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.
