A study for a 50 year old woman who takes Xyzal Allergy 24hr, Flonase, Singulair - from FDA reports


1,510 females aged 50 (±5) who take the same drugs are studied. This is a personalized study for a 50 year old female patient who has Allergy, Asthma. The study is created by eHealthMe based on reports from FDA.



On Apr, 16, 2018

1,510 females aged 50 (±5) who take Xyzal Allergy 24hr, Flonase, Singulair are studied.


Number of reports submitted per year:

Xyzal Allergy 24hr, Flonase, Singulair for a 50-year old woman.

Information of the patient in this study:

  • Age: 50
  • Gender: female
  • Conditions: Allergy, Asthma
  • Drugs taken:
    • Xyzal Allergy 24hr (levocetirizine dihydrochloride)
    • Flonase (fluticasone propionate)
    • Singulair (montelukast sodium)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Cough: 21 (1.39% of females aged 50 (±5) who take the drugs)

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 drug interactions over time

< 1 month:
  1. Dizziness
  2. Feeling abnormal
  3. Anaphylaxis (serious allergic reaction that is rapid in onset and may cause death)
  4. Oral disorder (mouth disease)
  5. Malaise (a feeling of general discomfort or uneasiness)
1 - 6 months:
  1. Allergic granulomatous angiitis (allergic inflammation of a blood vessel or lymph duct)
  2. Hypoaesthesia (reduced sense of touch or sensation)
  3. Abdominal pain upper
  4. Alanine aminotransferase increased
  5. Parosmia (distortion of the sense of smell, as in smelling odours that are not present)
6 - 12 months:
  1. Henoch-schonlein purpura (inflammation of the blood vessels in the skin and other body organs)
  2. Weight decreased
  3. Suicidal ideation
  4. Drug ineffective
  5. Dry mouth
1 - 2 years:
  1. Itching
  2. Hypoaesthesia (reduced sense of touch or sensation)
  3. Allergic granulomatous angiitis (allergic inflammation of a blood vessel or lymph duct)
  4. Hearing loss
  5. Urticaria (rash of round, red welts on the skin that itch intensely)
2 - 5 years:
  1. Depression
  2. Urticaria (rash of round, red welts on the skin that itch intensely)
  3. Stress and anxiety
  4. Hiatal hernia (hernia resulting from the protrusion of part of the stomach through the diaphragm)
  5. Breast cancer
5 - 10 years:
  1. Hyposmia (impairment of the sense of smell)
  2. Parosmia (distortion of the sense of smell, as in smelling odours that are not present)
  3. Smell - impaired
  4. Pulmonary embolism (blockage of the main artery of the lung)
  5. Migraine (headache)
10+ years:
  1. Loss of consciousness
  2. Nausea (feeling of having an urge to vomit)
  3. Nausea and vomiting
  4. Influenza like illness
  5. Arrhythmias (irregular heartbeat)
not specified:
  1. Breathing difficulty
  2. Nausea (feeling of having an urge to vomit)
  3. Fatigue (feeling of tiredness)
  4. Pain
  5. Headache (pain in head)

Top conditions involved for these people *:

  1. Hypersensitivity : 161 people, 10.66%
  2. Pain : 107 people, 7.09%
  3. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 105 people, 6.95%
  4. High Blood Pressure : 100 people, 6.62%
  5. Depression : 94 people, 6.23%

Top co-used drugs for these people *:

  1. Albuterol (263 people, 17.42%)
  2. Zyrtec (193 people, 12.78%)
  3. Xolair (185 people, 12.25%)
  4. Advair Diskus 100/50 (180 people, 11.92%)
  5. Nexium (175 people, 11.59%)

* 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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