A study for a 54 year old woman who takes Propranolol Hydrochloride - from FDA reports

4,410 females aged 54 (±5) who take the same drug are studied. This is a personalized study for a 54 year old female patient who has Hypertension. The study is created by eHealthMe based on reports from FDA.

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On May, 15, 2018

4,410 females aged 54 (±5) who take Propranolol Hydrochloride are studied.

Number of reports submitted per year:

Propranolol Hydrochloride for a 54-year old woman.

Information of the patient in this study:

  • Age: 54
  • Gender: female
  • Conditions: Hypertension
  • Drugs taken:
    • Propranolol Hydrochloride (propranolol hydrochloride)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Numbness In Feet: 0 (0% of females aged 54 (±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. Bradycardia (abnormally slow heart action)
  2. Fatigue (feeling of tiredness)
  3. Cardiogenic shock (inadequate circulation of blood)
  4. Headache (pain in head)
  5. Joint pain
1 - 6 months:
  1. Pancytopenia (medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets)
  2. Fever
  3. Breathing difficulty
  4. Feeling abnormal
  5. Swelling face
6 - 12 months:
  1. Hypoaesthesia (reduced sense of touch or sensation)
  2. Injury
  3. Pain
  4. Stroke (sudden death of a portion of the brain cells due to a lack of oxygen)
  5. Speech impairment (adult) (inability to speak (adult))
1 - 2 years:
  1. Rashes (redness)
  2. Subileus
  3. Balance disorder
  4. Tremor (trembling or shaking movements in one or more parts of your body)
  5. Oedema (fluid collection in tissue)
2 - 5 years:
  1. Weight increased
  2. Myocardial ischaemia (the blood flow through one or more of the blood vessels that lead to heart (coronary arteries) is decreased)
  3. Fatigue (feeling of tiredness)
  4. Prinzmetal angina (cardiac chest pain at rest that occurs in cycles)
  5. Rotator cuff syndrome (a spectrum of conditions affecting the rotator cuff tendons of the shoulder)
5 - 10 years:
  1. Hyperreflexia (overactive or over responsive reflexes)
  2. Muscle aches (muscle pain)
  3. Speech impairment (adult) (inability to speak (adult))
  4. Diplopia (double vision)
  5. Muscle spasms (muscle contraction)
10+ years:
  1. Renal disorder (kidney disease)
  2. Drug ineffective
  3. Road traffic accident
  4. Mental disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)
  5. Liver disorder (liver diseases)
not specified:
  1. Nausea (feeling of having an urge to vomit)
  2. Fatigue (feeling of tiredness)
  3. Headache (pain in head)
  4. Pain
  5. Weakness

Top conditions involved for these people *:

  1. Depression : 381 people, 8.64%
  2. High Blood Cholesterol : 230 people, 5.22%
  3. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 220 people, 4.99%
  4. Pain : 219 people, 4.97%
  5. Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 217 people, 4.92%

Top co-used drugs for these people *:

  1. Synthroid (286 people, 6.49%)
  2. Premarin (229 people, 5.19%)
  3. Omeprazole (211 people, 4.78%)
  4. Xanax (210 people, 4.76%)
  5. Nexium (186 people, 4.22%)

* 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).

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