A study for a 69 year old woman who takes Forteo, Doryx Mpc - from FDA reports


28 females aged 69 (±5) who take the same drugs are studied. This is a personalized study for a 69 year old female patient who has Osteoporosis, Cellulitis. The study is created by eHealthMe based on reports from FDA.

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


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On Jul, 21, 2018

28 females aged 69 (±5) who take Forteo, Doryx Mpc are studied.


Number of reports submitted per year:

Forteo, Doryx Mpc for a 69-year old woman.

Information of the patient in this study:

  • Age: 69
  • Gender: female
  • Conditions: Osteoporosis, Cellulitis
  • Drugs taken:
    • Forteo (teriparatide recombinant human)
    • Doryx Mpc (doxycycline hyclate)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Toothaches(tooth pain): 0 (0% of females aged 69 (±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:
n/a
1 - 6 months:
  1. Weight decreased
  2. Weakness
  3. Hypophagia (reduced food intake)
  4. Complex regional pain syndrome (long lasting pain condition most often affecting one of the limbs (arms, legs, hands, or feet))
  5. Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
  6. Hip fracture
  7. Blood glucose decreased
  8. Femur fracture
  9. Gait disturbance
  10. The flu (the flu is caused by an influenza virus)
6 - 12 months:
n/a
1 - 2 years:
  1. Dementia (madness)
  2. Dementia alzheimer's type (loss of mental ability with alzheimer's symptom)
2 - 5 years:
n/a
5 - 10 years:
n/a
10+ years:
n/a
not specified:
  1. Weakness
  2. Nausea (feeling of having an urge to vomit)
  3. Pain
  4. Eye pain
  5. Nausea and vomiting
  6. Eye disorder
  7. Dizziness
  8. Blepharitis (chronic inflammation of the eyelid)
  9. Weight decreased
  10. Blood glucose decreased

Top conditions involved for these people *:

  1. Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 2 people, 7.14%
  2. Open Fracture : 2 people, 7.14%
  3. Anaphylaxis (serious allergic reaction that is rapid in onset and may cause death): 2 people, 7.14%
  4. Systemic Sclerosis (Scleroderma) (an autoimmune or connective tissue disease. it is characterized by thickening of the skin): 1 person, 3.57%
  5. Stomatitis (inflammation of mucous membrane of mouth): 1 person, 3.57%
  6. Spinal Fracture (fracture in one of vertebrae): 1 person, 3.57%
  7. Pneumonia : 1 person, 3.57%
  8. Osteopenia (a condition where bone mineral density is lower than normal): 1 person, 3.57%
  9. Irritable Bowel Syndrome : 1 person, 3.57%
  10. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 1 person, 3.57%

Top co-used drugs for these people *:

  1. Singulair (6 people, 21.43%)
  2. Atenolol (5 people, 17.86%)
  3. Levaquin (3 people, 10.71%)
  4. Gabapentin (3 people, 10.71%)
  5. Hydroxyzine (3 people, 10.71%)
  6. Desonide (3 people, 10.71%)
  7. Levetiracetam (3 people, 10.71%)
  8. Lexapro (3 people, 10.71%)
  9. Lidex (3 people, 10.71%)
  10. Lorazepam (3 people, 10.71%)

* Some reports may have incomplete information.

You are not alone:

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Related studies:

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FDA reports used in this study


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

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

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

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