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From FDA reports: side effects of Apotex Fentanyl Transdermal System Man. By Hisamitsu for a Female patient aged 69

This is a personalized study for a 69 year old female patient. The study is created by eHealthMe based on reports of 60,821 people who take the same drug and have side effectsfrom FDA.

On Nov, 17, 2014: 60,821 people who reported to have side effects when taking Apotex Fentanyl Transdermal System Man. By Hisamitsu are studied

Trend of Apotex Fentanyl Transdermal System Man. By Hisamitsu's drug interactions, side effects, and effectiveness reports (3816379)

Information of the patient in this study:

Age: 69

Gender: female

Conditions: Pain

Drugs taking:
- Apotex Fentanyl Transdermal System Man. By Hisamitsu
- Apotex Fentanyl Transdermal System Man. By Hisamitsu

Side effects have: Economic Problem, Drug Effect Decreased, Complication Of Device Removal, Application Site Vesicles, Application Site Reaction, Application Site Erosion

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 69 (±5):

Side effectNumber of reports
Economic Problem18 (0.41%)
Drug Effect Decreased126 (2.90%)
Complication Of Device Removal2 (0.05%)
Application Site Vesicles (small bubble within a cell at application site)20 (0.46%)
Application Site Reaction30 (0.69%)
Application Site Erosion20 (0.46%)

Most common side effects experienced by females aged 69 (±5) in the use of Apotex Fentanyl Transdermal System Man. By Hisamitsu:

Side effectNumber of reports
Pain969
Nausea (feeling of having an urge to vomit)848
Anxiety662
Death645
Vomiting620
Wrong Technique In Drug Usage Process588
Asthenia (weakness)577
Fall564
Dyspnoea (difficult or laboured respiration)535
Back Pain494

Most common side effects experienced by females aged 69 (±5) in long term use of Apotex Fentanyl Transdermal System Man. By Hisamitsu:

Side effectNumber of reports
Death17
Constipation12
Somnolence (a state of near-sleep, a strong desire for sleep)11
Drug Dose Omission10
Dyspnoea (difficult or laboured respiration)10
Transient Ischaemic Attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))8
Vomiting8
Anxiety8
Headache (pain in head)8
Tremor (trembling or shaking movements in one or more parts of your body)8

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

Comparison with this patient's adverse outcomes:

Side effectNumber of reports
Economic Problem214 (0.35%)
Drug Effect Decreased2,810 (4.62%)
Complication Of Device Removal6 (0.01%)
Application Site Vesicles (small bubble within a cell at application site)442 (0.73%)
Application Site Reaction1,026 (1.69%)
Application Site Erosion232 (0.38%)

Most common side effects experienced by people in the use of Apotex Fentanyl Transdermal System Man. By Hisamitsu:

Side effectNumber of reports
Wrong Technique In Drug Usage Process12,920
Pain11,956
Nausea (feeling of having an urge to vomit)9,515
Death7,940
Anxiety7,887
Vomiting7,498
Drug Ineffective7,232
Product Quality Issue6,712
Dyspnoea (difficult or laboured respiration)5,975
Fall4,834

Most common side effects experienced by people in long term use of Apotex Fentanyl Transdermal System Man. By Hisamitsu:

Side effectNumber of reports
Pain184
Product Quality Issue160
Wrong Technique In Drug Usage Process152
Drug Ineffective140
Nausea (feeling of having an urge to vomit)122
Drug Withdrawal Syndrome (interfere with normal social, occupational, or other functioning. are not due to another medical condition, drug use, or discontinuation)106
Vomiting104
Dizziness93
Hyperhidrosis (abnormally increased sweating)90
Constipation88

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.

You can also:

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.

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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).

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

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