Spinraza

nusinersen
Antisense Oligonucleotide Biogen FDA Monitored

Safety Profile Overview

First approved treatment for spinal muscular atrophy. Administered intrathecally. Monitored for thrombocytopenia and renal toxicity.

Generic Name
nusinersen
Brand Names
Spinraza
Therapeutic Class
Antisense Oligonucleotide
Manufacturer
Biogen

What Pharma Signal Tracks for Spinraza

Data Disclaimer: Pharma Signal aggregates data from the FDA Adverse Event Reporting System (FAERS) and other public regulatory sources. FAERS reports do not establish causation. Report counts may reflect prescription volume rather than relative safety. Always consult healthcare professionals for medical decisions.

Get Spinraza Safety Data via API

One API call returns adverse events, risk scores, recalls, and pharmacovigilance signals for Spinraza.

curl "https://api.pharma-signal.com/drug/safety/spinraza" \
  -H "X-API-Key: your_key"

# Returns risk score, adverse event counts,
# serious/death rates, recalls, and signals

Related Safety Intelligence

Pharma Signal provides comparative analysis across therapeutic classes. Compare Spinraza against other Antisense Oligonucleotide drugs, or explore the full manufacturer portfolio for Biogen.