This
page
is
part
of
the
FHIR
Specification
(v4.3.0:
R4B
(v5.0.0-ballot:
R5
Ballot
-
STU
see
ballot
notes
).
The
current
version
which
supercedes
this
version
is
5.0.0
.
For
a
full
list
of
available
versions,
see
the
Directory
of
published
versions
.
Page
versions:
R5
R4B
| Biomedical Research and Regulation Work Group | Maturity Level : N/A | Standards Status : Informative | Compartments : Not linked to any defined compartments |
This is the narrative for the resource. See also the XML , JSON or Turtle format. This example conforms to the profile MedicinalProductDefinition .
Generated Narrative
Id : equilidem-basics
Identifier : Equilidem25
Combined Pharmaceutical Dose Form : tablet
Indication : Prevention of venous thromboembolic events (VTE) in adult patients who have undergone elective hip or knee replacement surgery. Prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (NVAF), with one or more risk factors, such as prior stroke or transient ischaemic attack (TIA); age ≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (NYHA Class >= II). Treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prevention of recurrent DVT and PE in adults.
Legal Status Of Supply : Prescription only medicine
Classification : ATC: B01A
Ingredient :
| - | Product Name |
| * | Equilidem 2.5 mg film-coated tablets |
| - | Product |
| * | Link to generic equivalent |
| - | Manufacturer |
| * | EquiliDrugCo Inc. |
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.