Teduglutide

Common brands: Gattex, Vitamin D, Acid Reducer, Imodium A-D, Foster And Thrive Acid Reducer

Top reporter: Takeda Pharmaceuticals America, Inc.

GLP-2 Analog [EPC]Provitamin D2 Compound [EPC]Proton Pump Inhibitor [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Osmotic Laxative [EPC]
13,200
Total Reports
9,031
Serious Reports
1,141
Death Reports
30
Reported Reactions
Death Report Ratio: High (8.64%)

Patient Demographics

Male
4,676
Female
7,545

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Teduglutide.

# Reaction Reports % of Total
1 WEIGHT DECREASED 1,242
6.4%
2 VASCULAR DEVICE INFECTION 1,151
6.0%
3 NAUSEA 1,082
5.6%
4 ABDOMINAL PAIN 1,045
5.4%
5 PRODUCT DOSE OMISSION ISSUE 1,044
5.4%
6 DIARRHOEA 1,031
5.3%
7 DEHYDRATION 868
4.5%
8 WEIGHT INCREASED 860
4.5%
9 VOMITING 834
4.3%
10 DEATH 771
4.0%
11 ABDOMINAL DISTENSION 708
3.7%
12 PYREXIA 615
3.2%
13 HOSPITALISATION 591
3.1%
14 INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION 537
2.8%
15 DECREASED APPETITE 518
2.7%
16 SEPSIS 515
2.7%
17 DEVICE RELATED INFECTION 506
2.6%
18 ABDOMINAL PAIN UPPER 485
2.5%
19 PRODUCT USE ISSUE 478
2.5%
20 FATIGUE 453
2.3%
21 PNEUMONIA 434
2.2%
22 DRUG INEFFECTIVE 414
2.1%
23 INTESTINAL OBSTRUCTION 411
2.1%
24 MALAISE 406
2.1%
25 PERIPHERAL SWELLING 393
2.0%
26 COVID-19 391
2.0%
27 FLATULENCE 387
2.0%
28 STOMA COMPLICATION 376
1.9%
29 URINARY TRACT INFECTION 376
1.9%
30 PAIN 369
1.9%

Important Disclaimer

FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.