Advair

N/A

Manufactured by GlaxoSmithKline LLC

20,040 FDA adverse event reports analyzed

Last updated: 2026-05-19

About Advair

Advair is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by GlaxoSmithKline LLC. The most commonly reported adverse reactions for Advair include DYSPNOEA, PNEUMONIA, DRUG INEFFECTIVE, ASTHMA, COUGH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for Advair.

Top Adverse Reactions

DYSPNOEA1,359 reports
PNEUMONIA724 reports
DRUG INEFFECTIVE701 reports
ASTHMA551 reports
COUGH543 reports
PRODUCT QUALITY ISSUE533 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE481 reports
PAIN439 reports
FATIGUE397 reports
NAUSEA391 reports
HEADACHE363 reports
DIZZINESS336 reports
MALAISE334 reports
DEATH333 reports
FALL308 reports
DIARRHOEA291 reports
OFF LABEL USE270 reports
ANXIETY268 reports
BRONCHITIS263 reports
VOMITING263 reports
ASTHENIA255 reports
ARTHRALGIA249 reports
CHEST PAIN241 reports
DYSPHONIA218 reports
PAIN IN EXTREMITY215 reports
BACK PAIN205 reports
INJECTION SITE PAIN204 reports
WEIGHT DECREASED204 reports
WHEEZING202 reports
CHEST DISCOMFORT196 reports
NASOPHARYNGITIS195 reports
PYREXIA191 reports
INSOMNIA186 reports
HYPERTENSION185 reports
RASH185 reports
DRUG DOSE OMISSION181 reports
MYOCARDIAL INFARCTION181 reports
SINUSITIS178 reports
DEPRESSION177 reports
FEELING ABNORMAL173 reports
DRUG ADMINISTRATION ERROR161 reports
PULMONARY EMBOLISM160 reports
ANAEMIA157 reports
PRURITUS150 reports
OEDEMA PERIPHERAL148 reports
TREMOR147 reports
CEREBROVASCULAR ACCIDENT145 reports
WEIGHT INCREASED144 reports
ABDOMINAL PAIN143 reports
OROPHARYNGEAL PAIN142 reports
MUSCLE SPASMS138 reports
GAIT DISTURBANCE136 reports
CATARACT135 reports
HOSPITALISATION135 reports
HYPOAESTHESIA132 reports
CARDIAC FAILURE CONGESTIVE130 reports
INJURY129 reports
GASTROOESOPHAGEAL REFLUX DISEASE127 reports
DECREASED APPETITE123 reports
ABDOMINAL PAIN UPPER120 reports
LUNG NEOPLASM MALIGNANT120 reports
URINARY TRACT INFECTION120 reports
RESPIRATORY FAILURE118 reports
CONSTIPATION117 reports
DEEP VEIN THROMBOSIS116 reports
HEART RATE INCREASED115 reports
INCORRECT ROUTE OF DRUG ADMINISTRATION115 reports
HYPERSENSITIVITY114 reports
ARTHRITIS112 reports
OSTEOPOROSIS112 reports
INVESTIGATION110 reports
DEHYDRATION109 reports
MYALGIA109 reports
LUNG INFECTION107 reports
LUNG DISORDER106 reports
ATRIAL FIBRILLATION104 reports
GASTROINTESTINAL HAEMORRHAGE104 reports
HYPOTENSION104 reports
OSTEOARTHRITIS103 reports
DIABETES MELLITUS102 reports
LOCAL SWELLING102 reports
VISION BLURRED101 reports
CONTUSION99 reports
INFECTION99 reports
PARAESTHESIA96 reports
BLOOD PRESSURE INCREASED95 reports
DRY MOUTH94 reports
PALPITATIONS94 reports
THROAT IRRITATION94 reports
INFLUENZA93 reports
CONDITION AGGRAVATED92 reports
GENERAL PHYSICAL HEALTH DETERIORATION92 reports
INCORRECT DOSE ADMINISTERED92 reports
OVERDOSE90 reports
CARDIAC DISORDER88 reports
DYSPHAGIA88 reports
EMOTIONAL DISTRESS87 reports
PRODUCTIVE COUGH86 reports
EMPHYSEMA85 reports
MEMORY IMPAIRMENT85 reports

Report Outcomes

Out of 8,891 classified reports for Advair:

  • Serious: 5,940 reports (66.8%) — includes hospitalization, disability, life-threatening events, or death
  • Non-Serious: 2,951 reports (33.2%)
Serious 66.8%Non-Serious 33.2%

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

Female6,029 (68.2%)
Male2,732 (30.9%)
Unknown74 (0.8%)

Reports by Age

Age 61196 reports
Age 64194 reports
Age 68177 reports
Age 66176 reports
Age 58175 reports
Age 63170 reports
Age 59156 reports
Age 62156 reports
Age 65154 reports
Age 73152 reports
Age 60148 reports
Age 69148 reports
Age 67144 reports
Age 70144 reports
Age 53143 reports
Age 56137 reports
Age 57137 reports
Age 55135 reports
Age 54134 reports
Age 71134 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 Advair?

This profile reflects 20,040 FDA FAERS reports that mention Advair. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for Advair?

Frequently reported terms in FAERS include DYSPNOEA, PNEUMONIA, DRUG INEFFECTIVE, ASTHMA, COUGH, PRODUCT QUALITY ISSUE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures Advair?

Labeling and FAERS entries often list GlaxoSmithKline LLC in connection with Advair. Always verify the specific product and NDC with your pharmacist.

Other Drugs by GlaxoSmithKline LLC

Explore other medications manufactured by GlaxoSmithKline LLC and compare their safety profiles:

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Drugs Also Linked to DYSPNOEA

The following drugs share commonly reported adverse reactions with Advair:

0XYGEN (75/100)ABEMACICLIB (78/100)ABIRATERONE ACETATE (72/100)ACALABRUTINIB (78/100)ACETAMINOPHEN (35/100)ACETAMINOPHEN 325 MG (65/100)ACETAMINOPHEN 325MG (65/100)ACETAMINOPHEN 500 MG (65/100)ACETAMINOPHEN 500MG (85/100)ACETAMINOPHEN AND CODEINE PHOSPHATE (85/100)ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE (72/100)ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE (65/100)

View all drugs reporting DYSPNOEA →

Explore More

Safety RankingsSearch All DrugsCompare DrugsGlaxoSmithKline LLC PortfolioDYSPNOEA in Other DrugsPNEUMONIA in Other DrugsDRUG INEFFECTIVE in Other Drugs
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.