NIGHTTIME COLD AND FLU RELIEF

N/A

Manufactured by Advanced Rx LLC

43 FDA adverse event reports analyzed

Last updated: 2026-04-14

About NIGHTTIME COLD AND FLU RELIEF

NIGHTTIME COLD AND FLU RELIEF is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Advanced Rx LLC. The most commonly reported adverse reactions for NIGHTTIME COLD AND FLU RELIEF include MIOSIS, NASOPHARYNGITIS, NAUSEA, ABDOMINAL ABSCESS, ACUTE SINUSITIS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NIGHTTIME COLD AND FLU RELIEF.

Top Adverse Reactions

MIOSIS2 reports
NASOPHARYNGITIS2 reports
NAUSEA2 reports
ABDOMINAL ABSCESS1 reports
ACUTE SINUSITIS1 reports
APPENDICITIS PERFORATED1 reports
ASTHMA1 reports
BACTERIAL INFECTION1 reports
BALANCE DISORDER1 reports
BURNING SENSATION1 reports
COVID 191 reports
DIZZINESS1 reports
DRUG INEFFECTIVE1 reports
DRUG INTERACTION1 reports
DYSPNOEA EXERTIONAL1 reports
ERYTHEMA1 reports
EXTRASYSTOLES1 reports
GASTROENTERITIS VIRAL1 reports
HALLUCINATION1 reports
HERPES ZOSTER1 reports
HYPERHIDROSIS1 reports
HYPERSENSITIVITY1 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION1 reports
INFLUENZA1 reports
INSURANCE ISSUE1 reports
MULTIPLE ALLERGIES1 reports
NERVE INJURY1 reports
PRODUCTIVE COUGH1 reports
PRURITUS1 reports
SEASONAL ALLERGY1 reports
SECRETION DISCHARGE1 reports
SINUS DISORDER1 reports
SINUSITIS1 reports
SPEECH DISORDER1 reports
SWOLLEN TONGUE1 reports
THROMBOSIS1 reports
TONGUE BITING1 reports
UPPER RESPIRATORY TRACT INFECTION1 reports
VIRAL INFECTION1 reports
VOMITING1 reports

Report Outcomes

Out of 9 classified reports for NIGHTTIME COLD AND FLU RELIEF:

Serious 77.8%Non-Serious 22.2%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female6 (66.7%)
Male3 (33.3%)

Reports by Age

Age 101 reports
Age 371 reports
Age 421 reports
Age 471 reports
Age 541 reports
Age 711 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with NIGHTTIME COLD AND FLU RELIEF?

This profile reflects 43 FDA FAERS reports that mention NIGHTTIME COLD AND FLU RELIEF. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for NIGHTTIME COLD AND FLU RELIEF?

Frequently reported terms in FAERS include MIOSIS, NASOPHARYNGITIS, NAUSEA, ABDOMINAL ABSCESS, ACUTE SINUSITIS, APPENDICITIS PERFORATED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures NIGHTTIME COLD AND FLU RELIEF?

Labeling and FAERS entries often list Advanced Rx LLC in connection with NIGHTTIME COLD AND FLU RELIEF. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.