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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.

FRAMYCETIN\SODIUM: 12 Adverse Event Reports & Safety Profile

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12
Total FAERS Reports
12 (100.0%)
Deaths Reported
4
Hospitalizations
12
As Primary/Secondary Suspect
4
Life-Threatening
4
Disabilities

Active Ingredient: FRAMYCETIN SULFATE\SODIUM PROPIONATE ·

What Are the Most Common FRAMYCETIN\SODIUM Side Effects?

#1 Most Reported
Joint stiffness
10 reports (83.3%)
#2 Most Reported
Injury
10 reports (83.3%)
#3 Most Reported
Infusion related reaction
10 reports (83.3%)

All FRAMYCETIN\SODIUM Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Hypercholesterolaemia 10 83.3% 10 2
Hypertension 10 83.3% 10 2
Infusion related reaction 10 83.3% 10 2
Injury 10 83.3% 10 2
Joint stiffness 10 83.3% 10 2
Hypersensitivity 8 66.7% 8 0
Hypoaesthesia 8 66.7% 8 0
Impaired healing 8 66.7% 8 0
Infection 8 66.7% 8 0
Irritable bowel syndrome 8 66.7% 8 0
Joint dislocation 8 66.7% 8 0
Joint range of motion decreased 8 66.7% 8 0
Knee arthroplasty 7 58.3% 7 0

Who Reports FRAMYCETIN\SODIUM Side Effects? Age & Gender Data

Gender: 100.0% female, 0.0% male. Average age: 43.7 years. Most reports from: CA. View detailed demographics →

What Is FRAMYCETIN\SODIUM Used For?

IndicationReports
Product used for unknown indication 10

Official FDA Label for FRAMYCETIN\SODIUM

Official prescribing information from the FDA-approved drug label.