A study for a 59 year old woman who takes Flonase - from FDA reports


9,297 females aged 59 (±5) who take the same drug are studied. This is a personalized study for a 59 year old female patient who has Bone And Joint Pain. The study is created by eHealthMe based on reports from FDA.



On Apr, 15, 2018

9,297 females aged 59 (±5) who take Flonase are studied.


Number of reports submitted per year:

Flonase for a 59-year old woman.

Information of the patient in this study:

  • Age: 59
  • Gender: female
  • Conditions: Bone And Joint Pain
  • Drugs taken:
    • Flonase (fluticasone propionate)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Pain - Joints: 244 (2.62% of females aged 59 (±5) who take the drug)

As an adverse outcome could be a symptom of a condition, additional studies are listed to help identify the cause: for example, regardless of which drug is taken, how many female HBP patients aged 50 (±5) have nausea

As an adverse outcome could be a side effect of a drug, additional studies are listed to help identify the cause: for example, how many female Aspirin users aged 50 (±5) have nausea

Most common side effects over time

< 1 month:
  1. Headache (pain in head)
  2. Dizziness
  3. Drug ineffective
  4. Rashes (redness)
  5. Nausea (feeling of having an urge to vomit)
1 - 6 months:
  1. Nausea (feeling of having an urge to vomit)
  2. Dizziness
  3. Muscle spasms (muscle contraction)
  4. Femur fracture
  5. Drug ineffective
6 - 12 months:
  1. Breathing difficulty
  2. Nosebleed (bleeding from nose)
  3. Pancreatic neoplasm (pancreatic tumour)
  4. Bile duct obstruction (blockage in the tubes that carry bile from the liver to the gallbladder)
  5. Headache (pain in head)
1 - 2 years:
  1. Malaise (a feeling of general discomfort or uneasiness)
  2. Smell - impaired
  3. Fatigue (feeling of tiredness)
  4. Hypoaesthesia (reduced sense of touch or sensation)
  5. Gastroesophageal reflux disease (a condition in which stomach contents leak backward from the stomach into the oesophagus)
2 - 5 years:
  1. Tooth loss
  2. Headache (pain in head)
  3. Dermatomyositis (inflammation of the skin and underlying muscle tissue, typically occurring as an autoimmune condition or associated with internal cancer)
  4. Aseptic necrosis (the death of bone tissue due to a lack of blood supply)
  5. Lung cancer - non-small cell (lung cancer)
5 - 10 years:
  1. Drug ineffective
  2. Dizziness
  3. Pleural effusion (water on the lungs)
  4. Spondyloarthropathy (any joint disease of the vertebral column)
  5. Lumbar spinal stenosis (a medical condition in which the spinal canal narrows and compresses the spinal cord and nerves at the level of the lumbar bone)
10+ years:
  1. Chest pain
  2. Asthma
  3. Headache (pain in head)
  4. Psychomotor hyperactivity (feelings of extreme restlessness)
  5. Chronic obstructive pulmonary disease (a progressive disease that makes it hard to breathe)
not specified:
  1. Breathing difficulty
  2. Nausea (feeling of having an urge to vomit)
  3. Drug ineffective
  4. Fatigue (feeling of tiredness)
  5. Headache (pain in head)

Top conditions involved for these people *:

  1. Asthma : 1,450 people, 15.60%
  2. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 697 people, 7.50%
  3. High Blood Pressure : 674 people, 7.25%
  4. Hypersensitivity : 665 people, 7.15%
  5. Pain : 657 people, 7.07%

Top co-used drugs for these people *:

  1. Singulair (1,285 people, 13.82%)
  2. Albuterol (998 people, 10.73%)
  3. Synthroid (885 people, 9.52%)
  4. Nexium (766 people, 8.24%)
  5. Lasix (688 people, 7.40%)

* Some reports may have incomplete information.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Want to find out more about the FDA reports used in the study? You can request them from FDA.

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NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.