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avacincaptad pegol

Sold as Izervay. First FDA approval 08/04/2023: 3 years on the US market.

This grade answers one narrow question: how strong is the public evidence and safety record behind this drug, and how clean is its money trail and court record? It is not a verdict on whether the drug is right for you.

C

Score breakdown (68/100)

Safety ×35%
A
Evidence ×25%
F
Regulatory ×15%
A
Money & lawsuits ×15%
C
Options ×10%
F

Safety: 100

Evidence: 21

Regulatory history: 90

Money & lawsuits: 70

Options: 40

What the FDA label says

Approved uses

Not available.

Contraindications

None listed.

Warnings and precautions

Not available.

Adverse reactions (label)

Not available.

Source: FDA SPL label, effective .

Side-effect reports sent to the FDA

These are counts of reports people filed, not rates of harm. Anyone can file one, and nobody checks whether the drug was the cause. Millions of doses are taken for every report sent, so the useful part is how this drug compares with the average across all drugs.

309reports that mention this drug
309of those blame this drug, not another one the person was taking
42%of reports describe a serious outcome, such as a hospital stay (average for all drugs: 57%)
1.6%of reports include a death, from any cause (average for all drugs: 9.1%)

Problems reported most often

Intercepted Product Preparation Error · 25Visual Impairment · 24Needle Issue · 23No Adverse Event · 22Off Label Use · 22Eye Pain · 21Vision Blurred · 21Endophthalmitis · 16Syringe Issue · 16Choroidal Neovascularisation · 14Eye Inflammation · 14Intraocular Pressure Increased · 14Product Temperature Excursion Issue · 13Vitritis · 13Device Issue · 11

Reports per year

2023202420252026
411011580

Source: the FDA's Adverse Event Reporting System (FAERS). Reports are voluntary and unverified. Drugs that are prescribed a lot, in the news, or in lawsuits attract more reports, so the percentages are compared with the whole database to correct for that partly, not fully.

Recalls and regulatory record

0recall actions on file
1 / 0brand / generic applications
1label changes since 2021
NoREMS program

Evidence base

7randomized trials (PubMed)
0systematic reviews
14registered trials
88%of completed trials posted results
21%terminated or withdrawn
100%industry-funded

Counts measure how much evidence exists and how transparent it is, not how big the benefit is. For that, ask your prescriber: if 100 people like me took this, how many would get better because of it, and how many would be harmed? (Doctors call these the "number needed to treat" and "number needed to harm.") It differs by condition and is the number drug ads leave out. Sources: PubMed, ClinicalTrials.gov.

Money and lawsuits

In 2024, drug companies reported $2,437,854 in payments to US physicians and hospitals tied to this drug across 9,300 transactions (Izervay $2,437,854).

No pending federal MDL names this drug or its brands.

Not named in any federal pharmaceutical settlement of $100M or more on record.

Sources: CMS Open Payments (Sunshine Act); Judicial Panel on Multidistrict Litigation pending docket list; DOJ settlements as tabulated on Wikipedia with links to the primary record. State-court and individual suits are not included.

Who takes it and what it costs

Not in the Medicare Part D spending file (typically hospital-administered or very new drugs).

Same-class alternatives

No same-class alternatives found in RxClass.

Questions to ask your prescriber

  1. The most-reported problems in FDA's adverse event data are intercepted product preparation error, visual impairment, needle issue, no adverse event. How would we recognize and handle those?
  2. Off-label use is among the most-reported items for this drug. Is my use on-label, and if not, what evidence supports it?
  3. There is no generic. Is there an older generic in the same class that works as well for my situation?
  4. The manufacturer pays physicians heavily to promote this drug. Have you received anything from them?
  5. What result are we expecting, by when, and what is the plan if it does not happen?
  6. If 100 people like me took this drug, how many would actually get better because of it, and how many would be harmed by it? (Doctors call these the number needed to treat and the number needed to harm.)