Does DOXYCYCLINE Cause Product use in unapproved indication? 755 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 755 reports of Product use in unapproved indication have been filed in association with DOXYCYCLINE (Doxycycline). This represents 4.3% of all adverse event reports for DOXYCYCLINE.
755
Reports of Product use in unapproved indication with DOXYCYCLINE
4.3%
of all DOXYCYCLINE reports
212
Deaths
319
Hospitalizations
How Dangerous Is Product use in unapproved indication From DOXYCYCLINE?
Of the 755 reports, 212 (28.1%) resulted in death, 319 (42.3%) required hospitalization, and 256 (33.9%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYCYCLINE. However, 755 reports have been filed with the FAERS database.
What Other Side Effects Does DOXYCYCLINE Cause?
Drug ineffective (2,238)
Off label use (1,630)
Nausea (1,391)
Vomiting (1,357)
Drug hypersensitivity (1,294)
Rash (1,267)
Headache (1,061)
Condition aggravated (1,052)
Malaise (994)
Fatigue (979)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which DOXYCYCLINE Alternatives Have Lower Product use in unapproved indication Risk?
DOXYCYCLINE vs DOXYCYCLINE HYCLATE
DOXYCYCLINE vs DOXYCYCLINE\DOXYCYCLINE HYCLATE
DOXYCYCLINE vs DOXYLAMINE
DOXYCYCLINE vs DOXYLAMINE\PYRIDOXINE
DOXYCYCLINE vs DRONABINOL