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From FDA reports: drug interactions between Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide for a Female patient aged 61

This is a personalized study for a 61 year old female patient. The study is created by eHealthMe based on reports of 2 people who take the same drugs and have drug interactionsfrom FDA.

On Aug, 30, 2014: 2 people who reported to have interactions when taking Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide are studied

Trend of Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide's drug interactions, side effects, and effectiveness reports (679710)

Information of the patient in this study:

Age: 61

Gender: female

Conditions: Dry Socket

Drugs taking:
- Neosporin: used for < 1 month
- Conjugated Estrogen
- Venlafaxine Hcl
- Verapamil
- Valdecoxib
- Alendronate Sodium
- Loratadine
- Prinzide
- Furosemide

Drug interactions have: Abscess Oral, Granuloma, Hyperplasia, Osteonecrosis, Post Procedural Complication, Procedural Site Reaction, Surgical Procedure Repeated

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 61 (±5):

InteractionNumber of reports
Abscess Oral (abscess in the mouth)2 (100.00%)
Granuloma (a small area of inflammation due to tissue injury)2 (100.00%)
Hyperplasia (enlargement of an organ or tissue)2 (100.00%)
Osteonecrosis (death of bone)2 (100.00%)
Post Procedural Complication2 (100.00%)
Procedural Site Reaction2 (100.00%)
Surgical Procedure Repeated2 (100.00%)

Most common interactions experienced by females aged 61 (±5) in the use of Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide:

InteractionNumber of reports
Osteonecrosis (death of bone)2
Granuloma (a small area of inflammation due to tissue injury)2
Gingival Hyperplasia (overgrowth of gums)2
Gingival Abscess (pus in gums)2
Postoperative Wound Complication2
Medication Error2
Procedural Site Reaction2
Post Procedural Complication2
Surgical Procedure Repeated2
Hyperplasia (enlargement of an organ or tissue)2

Most common interactions experienced by females aged 61 (±5) in long term use of Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Abscess Oral (abscess in the mouth)2 (100.00%)
Granuloma (a small area of inflammation due to tissue injury)2 (100.00%)
Hyperplasia (enlargement of an organ or tissue)2 (100.00%)
Osteonecrosis (death of bone)2 (100.00%)
Post Procedural Complication2 (100.00%)
Procedural Site Reaction2 (100.00%)
Surgical Procedure Repeated2 (100.00%)

Most common interactions experienced by people in the use of Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide:

InteractionNumber of reports
Osteonecrosis (death of bone)2
Granuloma (a small area of inflammation due to tissue injury)2
Gingival Hyperplasia (overgrowth of gums)2
Gingival Abscess (pus in gums)2
Postoperative Wound Complication2
Medication Error2
Procedural Site Reaction2
Post Procedural Complication2
Surgical Procedure Repeated2
Hyperplasia (enlargement of an organ or tissue)2

Most common interactions experienced by people in long term use of Neosporin, Conjugated Estrogen, Venlafaxine Hcl, Verapamil, Valdecoxib, Alendronate Sodium, Loratadine, Prinzide, Furosemide:

None.

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.

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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.

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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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