Who have Blood calcium decreased with Lotrimin - from FDA reports

Blood calcium decreased is found among people who take Lotrimin, especially for people who are female, 50-59 old also take medication Dilantin, and have Convulsion. This study is created by eHealthMe based on reports of 1,065 people who have side effects when taking Lotrimin from FDA, and is updated regularly.

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 Feb, 14, 2019

1,065 people reported to have side effects when taking Lotrimin.
Among them, 7 people (0.66%) have Blood calcium decreased

Number of reports submitted per year:

Could Lotrimin cause Blood calcium decreased?

Gender of people who have Blood calcium decreased when taking Lotrimin *:

  • female: 85.71 %
  • male: 14.29 %

Age of people who have Blood calcium decreased when taking Lotrimin *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 14.29 %
  • 40-49: 14.29 %
  • 50-59: 71.43 %
  • 60+: 0.0 %

Top conditions involved for these people *:

  1. Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 6 people, 85.71%
  2. Stress And Anxiety: 1 person, 14.29%
  3. Renal Cancer Metastatic (cancer of kidney spreads to other part): 1 person, 14.29%
  4. Rashes (redness): 1 person, 14.29%
  5. Pain: 1 person, 14.29%
  6. Mood Swings (an extreme or rapid change in mood): 1 person, 14.29%
  7. Insomnia (sleeplessness): 1 person, 14.29%
  8. High Blood Pressure: 1 person, 14.29%
  9. Haemoglobin Decreased: 1 person, 14.29%
  10. Fever: 1 person, 14.29%

Top co-used drugs for these people *:

  1. Acyclovir: 6 people, 85.71%
  2. Fluconazole: 6 people, 85.71%
  3. Ceftriaxone: 6 people, 85.71%
  4. Pepcid: 6 people, 85.71%
  5. Nystatin: 6 people, 85.71%
  6. Neurontin: 6 people, 85.71%
  7. Trileptal: 6 people, 85.71%
  8. Dilantin: 6 people, 85.71%
  9. Triamcinolone: 2 people, 28.57%
  10. Ativan: 1 person, 14.29%

Top other side effects for these people *:

  1. Alanine Aminotransferase Increased: 7 people, 100.00%
  2. Aspartate Aminotransferase Increased: 7 people, 100.00%
  3. Blood Glucose Increased: 7 people, 100.00%
  4. Hyperkalemia (damage to or disease of the kidney): 7 people, 100.00%
  5. Haemoglobin Decreased: 7 people, 100.00%
  6. Weakness: 6 people, 85.71%
  7. Haematocrit Decreased: 6 people, 85.71%
  8. Nausea (feeling of having an urge to vomit): 6 people, 85.71%
  9. Mouth Ulcers: 6 people, 85.71%
  10. Lymph Node Palpable: 6 people, 85.71%

* Approximation only. Some reports may have incomplete information.

Do you have Blood calcium decreased while taking Lotrimin?

You are not alone:

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Lotrimin side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Browse all side effects of Lotrimin
a b c d e f g h i j k l m n o p q r s t u v w x y z

What would happen?

Predict new side effects and undetected conditions when you take Lotrimin and have Blood calcium decreased

FDA reports used in this study

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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT 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).

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

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