Portland Oregon Medical Malpractice Attorney
Under Oregon law, a medical malpractice case is a negligence actions with a particularized standard of care. A healthcare provider must use the degree of care, skill, and diligence that an ordinarily careful physician or surgeon in the same or similar circumstances in the same or a similar community would use.
All states have similar standards, but medical malpractice continues to cause serious personal injury or wrongful death to tens of thousands of patients each year. Portland Oregon medical malpractice attorney Dane E. Johnson believes strongly in protecting patients’ when they suffer serious losses because of the medical system’s mistakes:
- misdiagnosis or failure to diagnose
- anesthesiological mistakes
- improper prescription or administration of medications
- improper use of medical devices
- defective medical devices
- failure to obtain informed consent
- failure to order diagnostic tests or consult specialists
- failure to monitor; post-operative infection
- incorrect treatment
Any type of medical negligence may cause serious injury or death. Complications of improper treatment or failure to diagnose may include:
- Appendicitis and Gastrointestinal Perforations
- Birth Injury
- Blood Clots (Pulmonary Emboli)
- Cancer
- Heart Attack/Disease
- Infection
- Surgical Error
If you have suffered due to misdiagnosis or surgical errors, our law firm may be able to help.
As an Oregon medical malpractice law firm, we must understand the medical complexities, make the medical evidence understandable to a jury, and change the attitudes that stand between the medical system and fair compensation for its failures.
If you or a loved one have suffered because of any form of medical malpractice or neglect, including misdiagnosis or failure to diagnose cancer; serious injury or wrongful death due to anesthesia, drugs, or medical devices; surgical procedures performed without consent; serious injury or wrongful death due to failure to order tests, consult specialists, or monitor patients; or incorrect treatment of any other kind, contact us. Your potential surgery error case can be evaluated by our Portland law firm at no cost.
Oregon medical misdiagnosis and surgical error attorney. Call us toll free (800) 714-3204.
Contact attorney Dane Johnson at (503) 975-8298 or contact us online for a free confidential initial consultation. There are no attorneys’ fees unless we recover compensation for you.
The Law Office of Dane E. Johnson is committed to providing resources to help reduce medical malpractice, improve medical device safety, and keep consumers aware of dangerous drugs and medical products. The following are the most recent MedWatch Safety Alerts available as published by the Food and Drug Administration (FDA):
MedWatch Safety Alert RSS Feed
FDA MedWatch Safety Alerts
Tygacil (tigecycline): Label Change – Increased Mortality Risk September 1, 2010
Source: MedWatch Safety Alert RSS Feed |
Huber Needles: Recall – Risk of Coring August 26, 2010
Source: MedWatch Safety Alert RSS Feed |
Fingerstick Devices to Obtain Blood Specimens: Initial Communication – Risk of Transmitting Bloodborne Pathogens August 26, 2010
Source: MedWatch Safety Alert RSS Feed |
TimeOut Capsules: Undeclared Drug Ingredient August 25, 2010
Source: MedWatch Safety Alert RSS Feed |
MasXtreme Capsules (Natural Wellness) – product contains undeclared drug ingredient August 25, 2010
Source: MedWatch Safety Alert RSS Feed |
Octagam (Immune Globulin Intravenous (human)) 5% Liquid Preparation: Market Withdrawal – Risk of Thromboembolic Events August 25, 2010
Source: MedWatch Safety Alert RSS Feed |
Mr. Magic Male Enhancer: Undeclared Drug Ingredient August 24, 2010
Source: MedWatch Safety Alert RSS Feed |
INOMAX DS Drug-Delivery System: Class I Recall – Risk of Interruption of Drug Flow August 24, 2010
Source: MedWatch Safety Alert RSS Feed |
Stalevo(carbidopa/levodopa and entacapone): Ongoing Safety Review: Possible increased cardiovascular risk August 20, 2010
Source: MedWatch Safety Alert RSS Feed |
Midodrine hydrochloride: FDA Proposes Withdrawal of Low Blood Pressure Drug August 16, 2010
Source: MedWatch Safety Alert RSS Feed |
6 French Engage Introducer Devices by St. Jude Medical: Recall – Potential for Separation of Shaft From Hub August 13, 2010
Source: MedWatch Safety Alert RSS Feed |
Prolatis’: Undeclared Drug Ingredient August 13, 2010
Source: MedWatch Safety Alert RSS Feed |
Lamictal (lamotrigine): Label Change – Risk of Aseptic Meningitis August 12, 2010
Source: MedWatch Safety Alert RSS Feed |
Novacare LLC Products: Recall – Undeclared Drug Ingredient August 11, 2010
Source: MedWatch Safety Alert RSS Feed |
Combat Application Tourniquets (C-A-T): Suspected Counterfeit Product August 9, 2010
Source: MedWatch Safety Alert RSS Feed |
Inferior Vena Cava (IVC) Filters: Initial Communication: Risk of Adverse Events with Long Term Use August 9, 2010
Source: MedWatch Safety Alert RSS Feed |
Solo Slim, Solo Slim Extra Strength: Recall – Undeclared Drug Ingredient August 9, 2010
Source: MedWatch Safety Alert RSS Feed |
Revivexxx Extra Strength: Recall – Undeclared Drug Ingredient August 9, 2010
Source: MedWatch Safety Alert RSS Feed |
Qualaquin (quinine sulfate): New Risk Evaluation and Mitigation Strategy – Risk of serious hematological reactions August 4, 2010
Source: MedWatch Safety Alert RSS Feed |
Cook brand Ciaglia Blue Rhino/Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays August 4, 2010
Source: MedWatch Safety Alert RSS Feed |





