GLP-1 FOIA Monitor — foiadocs.com
foiadocs.com · Live Monitor

GLP-1 FOIA Monitor

Every FDA FOIA Request Touching Semaglutide, Tirzepatide & the GLP-1 Class

594 FOIA Requests Track the GLP-1 Class

This tracker pulls every closed and open FDA FOIA request referencing semaglutide, tirzepatide, liraglutide, dulaglutide, exenatide, lixisenatide, or orforglipron — across all doc types, from adverse-event data pulls to approval packages to internal FDA correspondence.

53.9% Release Rate
320 released of 594
80 Currently Pending
Still open with FDA
138 Withdrawn
Often duplicate-scope closures
5.1 Years — Oldest Pending
Control #2021-4480

By Molecule

Drug / Brands All-Time Pending 2026 YTD
Semaglutide
Ozempic / Wegovy / Rybelsus
355 49 55
Tirzepatide
Mounjaro / Zepbound
189 25 31
Liraglutide
Victoza / Saxenda
74 11 20
Dulaglutide
Trulicity
21 3 10
Exenatide
Byetta / Bydureon
12 2 2
Orforglipron
Foundayo (oral, pending approval)
11 5 8
Lixisenatide
Adlyxin
3 0 2

Requests by Year

2020
3
2021
11
2022
9
2023
█████
45
2024
████████████████████████████████
281
2025
██████████████
121
2026
█████████████
115

Currently Pending — Oldest First

Showing 25 of 80 pending requests, sorted by how long they've been open. Rows shaded gold are 1+ years open; red are 2+ years.

Control # Requester Opened Days Open Subject
2021-4480 Young Andrew a Jul 9, 2021 1,850 sNDA -- Ozempic (Semaglutide) SUSTAIN-6 Trial Data (Dec 2016-2017)
2023-3195 Claire Fogarty Apr 27, 2023 1,193 FAERS -- Ozempic, Shortage and Off-Label Use
2023-8026 The Washington Post Sep 25, 2023 1,042 Correspondence -- FDA Drug Shortage Staff, Semaglutide/Tirzepatide (Mar 2022+)
2023-4774 Covington & Burling LLP Oct 6, 2023 1,031 Import -- Semaglutide Bulk Drug Substance (2021-Present)
2023-10439 Jennifer Thomas Nov 21, 2023 985 Correspondence -- Compounded Semaglutide (Apr 2023)
2024-3278 Bloomberg Apr 9, 2024 845 Correspondence -- FDA Communications on GLP-1 Drugs and Food Industry
2024-3364 Baker & Hostetler LLP Apr 11, 2024 843 Correspondence -- FDA-NABP Semaglutide and Tirzepatide (2022-2024)
2024-3365 Baker & Hostetler LLP Apr 11, 2024 843 Correspondence -- FDA-State Boards of Pharmacy, Semaglutide/Tirzepatide (2022-2024)
2024-3366 Baker & Hostetler LLP Apr 11, 2024 843 Correspondence -- Novo Nordisk Semaglutide Compounding (Jan 2022-Apr 2024)
2024-3367 Baker & Hostetler LLP Apr 11, 2024 843 Correspondence -- Eli Lilly Tirzepatide Compounding Communications (Jan 2022-Apr 2024)
2024-4841 Kff Health News Jun 3, 2024 790 Correspondence -- FDA Employees Semaglutide and Tirzepatide (Apr-May 2023)
2024-5064 Ragen Chastain Jun 11, 2024 782 sNDA -- Wegovy (Semaglutide 2.4mg) Cardiovascular Indication Approval
2024-6226 Baker & Hostetler LLP Jul 16, 2024 747 Correspondence -- Novo Nordisk, Eli Lilly, Julie Dohm Semaglutide/Tirzepatide Compounding (Jul 2022
2024-6273 Reuters Jul 17, 2024 746 Correspondence -- FDA-China NMPA Semaglutide Communications
2024-6275 Reuters Jul 17, 2024 746 Correspondence -- FDA-PMDA Semaglutide Communication (2019-present)
2024-6277 Reuters Jul 17, 2024 746 Correspondence -- Semaglutide and China (Jan 2019+)
2024-6278 Reuters Jul 17, 2024 746 Correspondence -- Semaglutide and India (Jan 2019 onwards)
2024-6372 Reuters Jul 18, 2024 745 Correspondence -- FDA-India CBIC Semaglutide (Jan 2019+)
2024-6373 Reuters Jul 18, 2024 745 Correspondence -- FDA-China Customs, Semaglutide (2019-present)
2024-8142 Pistevo Law LLC Sep 12, 2024 689 Correspondence -- Semaglutide and Tirzepatide Drug Shortage
2024-8180 Bloomberg News Sep 13, 2024 688 Correspondence -- Gail Bormel and Novo Nordisk/Eli Lilly (Compounded GLP-1 Drugs, 2022-)
2024-8181 Bloomberg News Sep 13, 2024 688 Correspondence -- FDA-Novo Nordisk/Eli Lilly GLP-1 Drug Shortages
2024-8331 Government Accountability Project Sep 20, 2024 681 Correspondence -- GLP-1 Agonists, Patient Access and Health Disparities
2025-188 Outsourcing Facilities Association Jan 6, 2025 573 Correspondence -- Eli Lilly Mounjaro/Zepbound/Tirzepatide Supply
2025-189 Outsourcing Facilities Association Jan 6, 2025 573 Correspondence -- Novo Nordisk Ozempic/Wegovy/Semaglutide Supply

Withdrawn Requests

Withdrawals are usually FDA closing a request as a duplicate of an existing one, or the requester narrowing scope after an initial broad filing. A late-2025 wave of Washington Post filings on GLP-1 intestinal-obstruction safety signals (labeling, FAERS, correspondence) were withdrawn in this pattern — worth noting since White Mountain Films is currently running a nearly identical set of pending requests on the same ileus/obstruction signal (EIR, label, and correspondence records for Novo Nordisk's Plainsboro, NJ site), suggesting overlapping investigative interest in that safety signal from two different requesters.

Control # Requester Opened Subject
2026-1502 Hyman Phelps & McNamara PC Feb 12, 2026 CRL -- Zepbound KwikPen (tirzepatide) NDA 217806 SUPPL-2 -- Complete Response Letter December 2, 2025
2026-1503 Hyman Phelps & McNamara PC Feb 12, 2026 ANDA -- 216418 -- Mercaptopurine Suspension 20 mg/mL -- Hikma Pharmaceuticals -- Bioequivalence and Biopharmaceutics
2026-822 The Wall Street Journal Jan 28, 2026 483 -- Seizure Logs & Laboratory Reports, Counterfeit Products (2024)
2026-790 Rbbins Geller Rudman & Dowd LLP Jan 27, 2026 Other -- GLP-1 Compounding Oversight & Enforcement (Jan 2023-Present)
2026-615 Dr Reddy's Laboratories Inc Jan 20, 2026 ANDA -- 214568 -- Liraglutide Solution Subcutaneous 18 mg/3 mL
2025-14048 The Washington Post Dec 15, 2025 Correspondence -- GLP-1 Drug Safety FDA Leadership Meetings (2022-2025)
2025-14049 The Washington Post Dec 15, 2025 Correspondence -- GLP-1 Drugs & GI Motility Injuries FDA-CDC (2021-2025)
CONS-2025-10 The Washington Post Dec 12, 2025 483 -- Novo Nordisk, Adverse Event Reporting Analysis (GLP-1 Products)
2025-13616 The Washington Post Dec 4, 2025 Correspondence -- GLP-1 Receptor Agonists, Labeling Changes (Jan 2020-Aug 2023)
2025-13302 The Washington Post Nov 26, 2025 Correspondence -- FDA Drug Safety Team, GLP-1 Receptor Agonists & Intestinal Obstruction (Oct 2022)
2025-13303 The Washington Post Nov 26, 2025 FAERS -- GLP1 Receptor Agonist, Intestinal Obstruction/Ileus Signal (Nov 2022)
2025-13306 The Washington Post Nov 26, 2025 Correspondence -- FDA Labeling Decision Process, GLP1 Receptor Agonist Ileus (Nov 2022-Sep 2023)
2025-13307 The Washington Post Nov 26, 2025 FAERS -- GLP-1 Receptor Agonists, Gastrointestinal Adverse Events (Novo Nordisk & Eli Lilly)
2025-13310 The Washington Post Nov 26, 2025 FAERS -- GLP-1 Receptor Agonists, Gastrointestinal Adverse Events (2022-present)
2025-13317 The Washington Post Nov 26, 2025 483 -- Novo Nordisk Inc., Plainsboro NJ (FEI 2244771)

Requester Landscape

Roughly a quarter of GLP-1 FOIA volume comes from press (gastrointestinal safety signals, compounding pharmacy coverage, shortage reporting). Plaintiff-side law firms — led by Morgan & Morgan, active in GLP-1 injury litigation — make up another large share, largely pulling FAERS adverse-event data and approval packages for discovery. One requester, FOIA Professional Services, has filed 81 near-identical FAERS pulls across a wide drug list including GLP-1s — consistent with a data-resale operation rather than a single case or story.

Media
████████████████████████
157
Law Firm
████████████████████████
158
FOIA Service (Competitor)
████████████
82
Industry
████████
54
Registered Agent Svc
██
13
Investment
4
Other/Individual
███████████████████
126

Top Individual Requesters

1
FOIA Professional Services (FOIA Service (Competitor))
82
2
Reuters (Media)
66
3
Morgan & Morgan PA (Law Firm)
48
4
27
5
26
6
22
7
15
8
Cogency Global Inc (Registered Agent Svc)
13
9
11
10
Barr & Gulyas (Law Firm)
9
11
9
12
Morgan & Morgan (Law Firm)
8
13
7
14
7
15
CBS News (Media)
6
16
Scripps News (Media)
5

What's Being Requested

████████████████████████
222
██████████
90
█████████
79
██████
55
█████
44
███
27
██
14
12
10
7
6
4
4
4
3
3
3
3
2
1
1

FAERS (adverse event) pulls dominate the GLP-1 request mix — a signal of ongoing safety-monitoring interest from press, plaintiff firms, and data resellers alike, well ahead of approval-package requests (NDA/ANDA/BLA).

Back to blog