| UNSAFE DRUGS |
| PRODUCT | MFG. | USE | INJURIES ALLEGED AS RESULT OF USE | CONTACT US IF: |
| Baxter Heparin |
Baxter International Inc. |
Anticoagulant, blood thinner. Commonly used before certain kinds of surgery. |
Anaphylactic shock with a signature injury of refractory hypotension (sudden drop in blood pressure) |
Baxter Heparin administered Oct. 2007 - March 1, 2008; and patient experienced either a drop in BP a short time after Heparin given, or immediate symptoms resulting in coma and death. |
| Fosamax |
Merck |
Postmenopausal osteoporosis |
Spontaneous fracture of the femur (thigh bone); Osteonecrosis of the jaw (ONJ) |
Patient suffered a spontaneous femur fracture or ONJ resulting in death. |
| Paxil |
GSK |
Depression, Anxiety |
Babies with birth defects; Suicide of a minor |
Patient's mother took Paxil and he/she was born with a congenital heart defect, persistent pulmonary hypertension or other birth defects. Patient was a minor and committed suicide after use of Paxil. |
| Gardasil Vaccine |
Various |
Various |
Acute Adverse Reaction |
Patient must have received a vaccination covered by the VICP (Vaccine Injury Compensation Program); adverse reaction must occur within weeks of the vaccination. Statute of limitations is 3 years from date of first adverse reaction; 2 years in the case of death. |
| DEFECTIVE MEDICAL DEVICES |
| PRODUCT | MFG. | USE | INJURIES ALLEGED AS RESULT OF USE | CONTACT US IF: |
| Medtronic Lead Wire |
Medtronic, Inc. |
Leads are thin insulated wires connected to a defibrillator that carry impulses to the heart. |
The Medtronic leads can fracture, resulting in repetitive and devastating electrical shocks to the patient. Resulting injuries include heart problems, death, shocking by device, required removal or capping of wires and replacement surgery. |
Patient has evidence of a lead fracture and/or wire replacement or capped wire. |
| Stryker Hip |
Stryker Howmedica Corp. |
Hip replacement |
The Stryker Hip Implant component recall involves two hip replacement cups - the Trident Acetabular PSL Cup and the Trident Hemispherical Cups. These cups can fail, causing pain and requiring repair surgery. |
Patient has evidence that one of the recalled Stryker Hip replacement cups has failed. |
| Zimmer Durom Cup Hip Socket Implant |
Zimmer Holdings |
Hip replacement |
Hip socket implant is failing. Patients may be required to undergo hip replacement surgery as a result. |
Patient has evidence that a Zurom Durom Cup implant has failed. |
| Composix Kugel Hernia Patch |
Bard Davol |
Used in hernia repair surgery (ventral, incisional and/or abdominal hernias) |
Bowel perforation; bowel obstruction or strangulation; sepsis; peritonitis; severe adhesions;other serious abdominal/digestive injuries; can result in death |
Date of implant between 1/2001 - 1/2007 and mesh was removed in full or part less than 2 years ago. Patient has injury as listed. |