Fortum 1 g powder for solution for injection or infusion – patient leaflet, side effects, dosage
Medicine status: No longer supplied Details
- Medicine strength:
- 1 g
- Still supplied:
-
- Ceftazidime 1 g powder for solution for injection/infusion
- Ceftazidime 1 g powder for solution for injection or infusion
- Ceftazidime 1.0 g powder for solution for injection or infusion (SmPC only)
- Ceftazidime Venus Pharma 1 g powder for solution for injection/infusion (SmPC only)
- Other strengths and forms:
- Contains active substance:
- ATC code:
- Similar medicines:
Sources: Original (products.mhra.gov.uk)
Facts about Fortum 1 g powder for solution for injection or infusion
| Active substance | Ceftazidime |
|---|---|
| Strength | 1 g |
| Pharmaceutical form | Powder for solution for injection Vials containing white to cream sterile powder. |
| How is it taken | Intravenous, Intramuscular |
| Excipients | Sodium carbonate (anhydrous sterile) |
| Is it available? | No, all its packs are listed as discontinued (NHS Dictionary of Medicines and Devices – not a record of current supplies) |
| Shelf life | 3 years After reconstitution: Chemical and physical in-use stability has been demonstrated for 6 days at 4°C and 9 hours at 25°C. From a microbiological point of view, the reconstituted solution should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at 2 to 8°C, unless reconstitution has taken place in controlled and validated aseptic conditions. After dilution: Chemical and physical in-use stability has been demonstrated for 6 days at 4°C and 9 hours at 25°C. From a microbiological point of view, the reconstituted and diluted solution should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at 2 to 8°C, unless reconstitution has taken place in controlled and validated aseptic conditions. |
| Storage | Store below 25°C. Keep vials in the outer carton to protect from light. For storage conditions after reconstitution see section 6.3. |
| Drug group (ATC) | Antibacterials for systemic use |
| Marketing authorisation | PL 48870/0035 (first authorised 17 October 1983) |
| Marketing authorisation holder | Sandoz Pharmaceuticals d.d. |
| Codes | BNF 05010201 |
Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.
