Does DOXYCYCLINE Cause Product dose omission issue? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Product dose omission issue have been filed in association with DOXYCYCLINE (Doxycycline). This represents 0.4% of all adverse event reports for DOXYCYCLINE.
68
Reports of Product dose omission issue with DOXYCYCLINE
0.4%
of all DOXYCYCLINE reports
4
Deaths
25
Hospitalizations
How Dangerous Is Product dose omission issue From DOXYCYCLINE?
Of the 68 reports, 4 (5.9%) resulted in death, 25 (36.8%) required hospitalization, and 1 (1.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYCYCLINE. However, 68 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DOXYCYCLINE Alternatives Have Lower Product dose omission issue Risk?
DOXYCYCLINE vs DOXYCYCLINE HYCLATE
DOXYCYCLINE vs DOXYCYCLINE\DOXYCYCLINE HYCLATE
DOXYCYCLINE vs DOXYLAMINE
DOXYCYCLINE vs DOXYLAMINE\PYRIDOXINE
DOXYCYCLINE vs DRONABINOL