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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DEVICE\GELATIN for Tissue sealing: Side Effects & Safety Data

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There are 18 adverse event reports in the FDA FAERS database where DEVICE\GELATIN was used for Tissue sealing.

Most Reported Side Effects for DEVICE\GELATIN

Side Effect Reports % Deaths Hosp.
Hypotension 20 41.7% 0 0
Tachycardia 20 41.7% 0 0
Adverse reaction 19 39.6% 0 0
Anaphylactic reaction 19 39.6% 0 0
Anaphylactic shock 19 39.6% 0 0
Angiopathy 19 39.6% 0 0
Back pain 19 39.6% 0 0
Blood pressure increased 19 39.6% 0 0
Emphysema 19 39.6% 0 0
Epistaxis 19 39.6% 0 0
Face oedema 19 39.6% 0 0
Flatulence 19 39.6% 0 0
Haemorrhage 19 39.6% 0 0
Haemothorax 19 39.6% 0 0
Hypersensitivity 19 39.6% 0 0

Other Indications for DEVICE\GELATIN

Transcatheter arterial chemoembolisation (11) Embolism (6) Product used for unknown indication (5)

Other Drugs Used for Tissue sealing

FIBRINOGEN HUMAN\THROMBIN HUMAN (226) APROTININ\CALCIUM\FIBRINOGEN HUMAN\FACTOR XIII CONCENTRATE \THROMBIN (14) FIBRINOGEN HUMAN\HUMAN THROMBIN (11) THROMBIN (10) APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN (8)

Related Pages

DEVICE\GELATIN Full Profile All Tissue sealing Drugs DEVICE\GELATIN Demographics DEVICE\GELATIN Timeline