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From FDA reports: side effects of Posterior Tibialis Tendon - Mtf, Human Allograft

This is a study of Posterior Tibialis Tendon - Mtf, Human Allograft side effects. The study is created by eHealthMe based on reports of 11,511 people who take the same drug and have side effectsfrom FDA.

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On Aug, 15, 2014: 11,511 people who reported to have side effects when taking Posterior Tibialis Tendon - Mtf, Human Allograft are studied

Trend of Posterior Tibialis Tendon - Mtf, Human Allograft's drug interactions, side effects, and effectiveness reports (3081072)

Information of the patient in this study:

Conditions: Soft Tissue Disorder

Drugs taking:
- Posterior Tibialis Tendon - Mtf, Human Allograft

Side effects have: Infection

eHealthMe real world results:

For people in general (regardless of gender or age):

Comparison with this patient's adverse outcomes:

Side effectNumber of reports
Infection380 (3.30%)

Most common side effects experienced by people in the use of Posterior Tibialis Tendon - Mtf, Human Allograft:

Side effectNumber of reports
Pyrexia (fever)2,451
Hiv Infection Nos1,442
Hiv Test Positive1,152
Nausea (feeling of having an urge to vomit)965
Hepatitis C964
Thrombocytopenia (decrease of platelets in blood)825
Renal Failure Acute (rapid kidney dysfunction)728
Condition Aggravated (worse condition)694
Drug Ineffective688
Haemoglobin Decreased658

Most common side effects experienced by people in long term use of Posterior Tibialis Tendon - Mtf, Human Allograft:

Side effectNumber of reports
Hepatitis C24
Hiv Infection22
Hypoglycaemia (deficiency of glucose in the bloodstream)18
Pyrexia (fever)18
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)12
Hepatitis B10
Malaise (a feeling of general discomfort or uneasiness)10
Hypoalbuminaemia (levels of albumin in blood serum are abnormally low)8
Hepatitis A8

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DISCLAIMER: All material available on 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 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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