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To evaluate the long-term safety of AJOVY in patients under actual use conditions and to specifically evaluate cardiovascular events. In addition, information on efficacy will be collected.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Drug | Ajovy syringe for SC injection 225 mg. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fremanezumab 225 Mg/1.5 mL Subcutaneous Solution | Drug | The usual adult dose is 225 mg of fremanezumab (genetical recombination) administered subcutaneously as a single dose once every 4 weeks or 675 mg administered subcutaneously as a single dose once every 12 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| Safety information (Adverse Event) | Any untoward medicinal occurrence in a patient or clinical study subject administered a Medicinal Product and which does not necessarily have a causal relationship with this treatment (see Annex â…£, ICH-E2A Guideline). An Adverse Event can therefore be any unfavorable and unintended sign (e.g. abnormal laboratory finding), symptom, or disease temporally associated with the use of a Medicinal Product, whether or not it is considered causally related to the Medicinal Product. | 2 years from the start date of treatment |
| Number of Special Situations | Collecting any Situations related to the use of an Otsuka product which may or may not be associated with an adverse event:
| 2 years from the start date of treatment |
| Number of off-Label Use | Collecting any type of off-Label Use that refers to situations where a product is intentionally used for a medical purpose not in accordance with the authorized product information. Off-label use also includes the intentional use in non-authorized population categories not indicated in the label. | 2 years from the start date of treatment |
| Incidence of Serious Adverse Event (e.g. resulting in death or life-threatening) | Collecting the number of any adverse drug experience/event occurring at any dose which
|
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Inclusion Criteria:
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Exclusion Criteria:
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Patients in Japan who are planned to be newly started on Ajovy syringe for SC injection 225 mg therapy for the suppression of migraine attacks
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Pharmacovigilance Department Otsuka Pharmaceutical Co., Ltd | Contact | +81-6-6943-7722 | komaniwa.satoshi@otsuka.jp |
| Name | Affiliation | Role |
|---|---|---|
| Yasuhiko Fukuta, PhD | Otsuka Pharmaceutical Co., Ltd. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pharmacovigilance Department | Recruiting | Osaka | 540-0021 | Japan |
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| ID | Term |
|---|---|
| D008881 | Migraine Disorders |
| ID | Term |
|---|---|
| D051270 | Headache Disorders, Primary |
| D020773 | Headache Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| ID | Term |
|---|---|
| C000604315 | fremanezumab |
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| 2 years from the start date of treatment |
| Incidence of Non-serious Adverse Events (i.e. all Adverse Events that do not meet the definition of a serious Adverse Event) | Collecting the number of non-serious Adverse Events | 2 years from the start date of treatment |
| D009422 | Nervous System Diseases |