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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.

Does MINIVELLE Cause Product quality issue? 201 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Product quality issue have been filed in association with MINIVELLE. This represents 48.4% of all adverse event reports for MINIVELLE.

201
Reports of Product quality issue with MINIVELLE
48.4%
of all MINIVELLE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product quality issue From MINIVELLE?

Of the 201 reports, 1 (0.5%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINIVELLE. However, 201 reports have been filed with the FAERS database.

What Other Side Effects Does MINIVELLE Cause?

No adverse event (125) Drug ineffective (106) Wrong technique in drug usage process (97) Off label use (93) Drug prescribing error (74) Hot flush (54) Incorrect drug administration duration (38) Drug dose omission (29) Application site erythema (26) Headache (15)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which MINIVELLE Alternatives Have Lower Product quality issue Risk?

MINIVELLE vs MINOCYCLINE MINIVELLE vs MINOCYCLINE\MINOCYCLINE MINIVELLE vs MINODRONIC ACID MINIVELLE vs MINOXIDIL MINIVELLE vs MIPOMERSEN

Related Pages

MINIVELLE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue MINIVELLE Demographics