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Alloderm Side Effects

Report Alloderm Side Effects

If you experienced any harmful or unwanted effects of Alloderm, please share your experience. This could help to raise awareness about Alloderm side effects, identify uknown risks and inform health professionals and patients taking Alloderm.

Examples: headache, dizziness


The most commonly reported Alloderm side effects are:
Pain (10 reports)
Failure Of Implant (7 reports)
Pain And Swelling (5 reports)
Rashes (4 reports)
Swelling (4 reports)
Itching (3 reports)
Itching,rash (3 reports)
Failure To Hold Pelvic Floor (1 reports)
HIGH FEVER 102.7 F HEADACHE NAUSEA (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.


To view a complete list of submitted side effects, please follow the link Alloderm side effects . You can also compare Alloderm side effects or view FDA reports.

Alloderm Side Effects reported to FDA

The following Alloderm reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Alloderm on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

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Mastitis, Graft Complication
on May 02, 2013 Female from US , 65 years of age, was treated with Alloderm. Directly after, patient experienced the unwanted or unexpected Alloderm side effects: mastitis, graft complication. Alloderm dosage: N/A.
Associated medications used:

Erythema, Epidermolysis
Patient was taking Alloderm Rtu (acellular Human Skin Graft). Patient felt the following Alloderm side effects: erythema, epidermolysis on Apr 18, 2013 from US Additional patient health information: Female , 60 years of age, was diagnosed with and. Alloderm Rtu (acellular Human Skin Graft) dosage: N/A.

Urticaria, Weight Decreased, Anaemia, Laboratory Test Abnormal
Adverse event was reported on Apr 02, 2013 by a Female taking Alloderm (Dosage: N/A) was diagnosed with and. Location: US , 48 years of age, weighting 105.0 lb, After Alloderm was administered, patient encountered several Alloderm side effects: urticaria, weight decreased, anaemia, laboratory test abnormal.

Breast Cellulitis, Post Procedural Infection
on Mar 04, 2013 Female from US , 51 years of age, was treated with Alloderm. Directly after, patient experienced the unwanted or unexpected Alloderm side effects: breast cellulitis, post procedural infection. Alloderm dosage: N/A.


Graft Complication
on Jan 29, 2013 Female from US , 59 years of age, was treated with Alloderm. Patient felt the following Alloderm side effects: graft complication. Alloderm dosage: N/A.

Breast Cellulitis, Product Quality Issue, Graft Infection, Transplant Failure
Patient was taking Alloderm. After Alloderm was administered, patient encountered several Alloderm side effects: breast cellulitis, product quality issue, graft infection, transplant failure on Feb 25, 2013 from US Additional patient health information: Female , 72 years of age, . Alloderm dosage: N/A.

Oedema, Purulence, Erythema, Induration, Wound Drainage
Adverse event was reported on Jan 04, 2013 by a Female taking Alloderm Rtu (acellular Human Skin Graft) (Dosage: Lot# B46695r-024 Exp. Date 06/2014) . Location: US , 44 years of age, Directly after, patient experienced the unwanted or unexpected Alloderm side effects: oedema, purulence, erythema, induration, wound drainage.

Breast Cellulitis, Graft Complication, Graft Infection
on Feb 11, 2013 Female from US , 72 years of age, was treated with Alloderm Rtu (acellular Human Skin Graft). Patient felt the following Alloderm side effects: breast cellulitis, graft complication, graft infection. Alloderm Rtu (acellular Human Skin Graft) dosage: N/A.

Skin Graft Infection, Product Quality Issue
on Dec 31, 2012 Female from US , 40 years of age, was treated with Alloderm Rtu (acellular Human Skin Graft). After Alloderm was administered, patient encountered several Alloderm side effects: skin graft infection, product quality issue. Alloderm Rtu (acellular Human Skin Graft) dosage: Alloderm (try (acellular Human Skin Graft).

Skin Graft Infection, Product Quality Issue
Patient was taking Alloderm Rtu (acellular Human Skin Graft). Directly after, patient experienced the unwanted or unexpected Alloderm side effects: skin graft infection, product quality issue on Jan 17, 2013 from US Additional patient health information: Female , 40 years of age, . Alloderm Rtu (acellular Human Skin Graft) dosage: N/A.

Breast Cellulitis, Implant Site Effusion
Adverse event was reported on Dec 26, 2012 by a Female taking Alloderm (Dosage: N/A) . Location: US , 73 years of age, Patient felt the following Alloderm side effects: breast cellulitis, implant site effusion.

Cellulitis
on Dec 26, 2012 Female from US , 58 years of age, was treated with Alloderm. After Alloderm was administered, patient encountered several Alloderm side effects: cellulitis. Alloderm dosage: N/A.

Cellulitis, Fluid Retention
on Dec 31, 2012 Female from US , 60 years of age, was treated with Alloderm. Directly after, patient experienced the unwanted or unexpected Alloderm side effects: cellulitis, fluid retention. Alloderm dosage: Lot # B46102r-006?exp Date 05/31/2014.

Graft Infection, Graft Complication, Product Quality Issue
Patient was taking Alloderm. Patient felt the following Alloderm side effects: graft infection, graft complication, product quality issue on Jan 14, 2013 from US Additional patient health information: Female , 62 years of age, . Alloderm dosage: N/A.

Infection, Transplant Rejection
Adverse event was reported on Aug 21, 2012 by a Female taking Alloderm (Dosage: Alot No.: B39248-004, Exp. Date: 07/31/2012) . Location: COUNTRY NOT SPECIFIED , 58 years of age, After Alloderm was administered, patient encountered several Alloderm side effects: infection, transplant rejection.

Open Wound, Breast Swelling, Staphylococcus Test Positive, Postoperative Wound Complication, Infection, Erythema, Breast Discharge, White Blood Cell Count Increased, Product Contamination Microbial
on Mar 19, 2012 Female from UNITED STATES , 76 years of age, was treated with Alloderm Rtu (acellular Human Skin Graft). Directly after, patient experienced the unwanted or unexpected Alloderm side effects: open wound, breast swelling, staphylococcus test positive, postoperative wound complication, infection, erythema, breast discharge, white blood cell count increased, product contamination microbial. Alloderm Rtu (acellular Human Skin Graft) dosage: N/A.

Postoperative Wound Infection, Wound Infection Staphylococcal
on Jan 25, 2011 Male from UNITED STATES , weighting 300.0 lb, was diagnosed with and was treated with Alloderm 8x16 X-thick Lifecell. Patient felt the following Alloderm side effects: postoperative wound infection, wound infection staphylococcal. Alloderm 8x16 X-thick Lifecell dosage: N/A. Patient was hospitalized.

Impaired Healing, Postoperative Wound Complication, Product Quality Issue, Purulent Discharge, Skin Graft Infection, Staphylococcal Skin Infection
Patient was taking Alloderm Life-cell. After Alloderm was administered, patient encountered several Alloderm side effects: impaired healing, postoperative wound complication, product quality issue, purulent discharge, skin graft infection, staphylococcal skin infection on Jul 19, 2010 from UNITED STATES Additional patient health information: Female , weighting 128.0 lb, was diagnosed with and. Alloderm Life-cell dosage: N/A.
Multiple concurrent drugs taken:

Post Procedural Infection, Skin Graft Infection
Adverse event was reported on Dec 02, 2009 by a Female taking Alloderm (acellular Human Skin Graft) (Dosage: N/A) . Location: UNITED STATES , 48 years of age, Directly after, patient experienced the unwanted or unexpected Alloderm side effects: post procedural infection, skin graft infection.

Graft Infection, Post Procedural Infection, Product Quality Issue
on Dec 02, 2009 Female from UNITED STATES , 49 years of age, was treated with Alloderm (acellular Human Skin Graft). Patient felt the following Alloderm side effects: graft infection, post procedural infection, product quality issue. Alloderm (acellular Human Skin Graft) dosage: N/A.

Graft Infection, Post Procedural Infection, Product Quality Issue
on Dec 02, 2009 Female from UNITED STATES , 66 years of age, was treated with Alloderm (acellular Human Skin Graft) 2830069-062. After Alloderm was administered, patient encountered several Alloderm side effects: graft infection, post procedural infection, product quality issue. Alloderm (acellular Human Skin Graft) 2830069-062 dosage: N/A.

Post Procedural Infection
Patient was taking Alloderm (acellular Human Skin Graft). Directly after, patient experienced the unwanted or unexpected Alloderm side effects: post procedural infection on Dec 02, 2009 from UNITED STATES Additional patient health information: Female , 51 years of age, . Alloderm (acellular Human Skin Graft) dosage: N/A.

Post Procedural Infection
Adverse event was reported on Dec 02, 2009 by a Female taking Alloderm (acellular Human Skin Graft) (Dosage: N/A) . Location: UNITED STATES , 54 years of age, Patient felt the following Alloderm side effects: post procedural infection.

Postoperative Wound Infection
on Sep 21, 2009 Female from UNITED STATES , 47 years of age, was treated with Alloderm (acellular Human Tissue Skin Graft). After Alloderm was administered, patient encountered several Alloderm side effects: postoperative wound infection. Alloderm (acellular Human Tissue Skin Graft) dosage: N/A.

Breast Disorder Female, Culture Positive, Device Malfunction, Purulence, Seroma, Serratia Infection, Surgical Procedure Repeated
on Jan 07, 2008 Female from UNITED STATES , 29 years of age, was treated with Alloderm (acellular Human Tissue Skin Graft). Directly after, patient experienced the unwanted or unexpected Alloderm side effects: breast disorder female, culture positive, device malfunction, purulence, seroma, serratia infection, surgical procedure repeated. Alloderm (acellular Human Tissue Skin Graft) dosage: N/A. Patient was hospitalized.

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Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Alloderm

Side Effects reported to FDA: 62

Alloderm safety alerts: No

Reported deaths: 1

Reported hospitalizations: 8

Latest Alloderm clinical trials