I disagree with the bolded. This particular vaccine hasn't been around long enough to make that determination and there are plenty of information on some pretty bad effects from those who took the vaccine.
While I agree that there is no reason to sue, I think reporting to to the medical board is the right thing to do. A medication was given without consent and while it did no harm to the patient it very easily could have.
As far as this vaccine being well studied, how do we know the long term effects of it?
Personally I would have a huge problem with this, and I would report it. To me its the responsible thing to do, who knows how many times this has happened previously or will happen again, maybe next time the patient would have some serious side effects because of a mistake like this.
Just curious, do you believe that (the bolded part ) makes it alright that the patient was given not give the depo when she was supposed to be?
To answer your last question first; NO, I do not believe that even giving an aspirin wrongly is okay. It was an error. The results of this error however is a non event. There was no harm and no injury. The doctor's office was very forthcoming about what happened, apologized, they have documented it in the clinical record. What would be the purpose of reporting this to any licensing agency? With regard to the safety of the vaccine. I believe that the following information is very reliable. I also feel that the bolded part, the recognition that the vaccine is so worthwhile and valuable, that the clinical trials were stopped so that those girls receiving the placebo could be protected is very telling. The issue with this young lady in question is, will there be a benefit to her since she has been sexually active and may have already been exposed to the viruses that the vaccine is designed to protect her against. The other issue with regard to 'safety', is not the long term effects down the road but how long the protective ability of the vaccine will last. Will there need to be revaccination? I don't know the answer to that.
Merck & Co. conducted a Phase III study named FUTURE II. This clinical trial was a randomized double-blind study with one controlled placebo group and one vaccination group. Over 12,000 women aged 1626 from thirteen countries participated in the study. Each woman was injected with either Gardasil or a placebo on Day 1, Month 2, and Month 6. In total, 6,082 women were given Gardasil and 6,075 received the placebo. Merck has tested the vaccine in several hundred 11- and 12-year-old girls.
On February 27, 2006, the independent Data and Safety Monitoring Board recommended the clinical trials be terminated on ethical grounds, so that young women on placebo could receive Gardasil.
As of February 2009, 40 million doses of Gardasil had been distributed worldwide, with no evidence the vaccine has caused serious adverse effects. According to the Centers for Disease Control, the vaccine was tested in over 11,000 women and girls (ages 9 to 26). The Food and Drug Administration and Centers for Disease Control say that the vaccine has only minor side effects, such as soreness around the injection area. The FDA and CDC consider the vaccine to be safe. It does not contain mercury, thiomersal or live virus or dead virus, only virus-like particles, which cannot reproduce in the human body.
Of the 23 million doses of Gardasil administered to girls and women up to December 31, 2008, 11,916 adverse events were reported to the Vaccine Adverse Event Reporting System (VAERS): 94% of these events have been classified as non-serious with the remaining 6% classified as serious. Gardasil has less than half the average percentage of serious reports. These are anecdotal reports, and "it is important to note that a report to VAERS does not mean there is a connection between the vaccine and the event. It means the event took place following vaccination."The FDA and CDC said that with millions of vaccinations by chance alone some serious adverse effects and deaths will occur in the time period following vaccination, but have nothing to do with the vaccine.Although at least 20 women who received the Gardasil vaccine have died, there is no evidence that deaths or serious outcomes were connected to the shot. Where information was available, the cause of death was explained by other factors. Likewise, although a small number of cases of Guillain-Barré Syndrome (GBS) have been reported following vaccination with Gardasil. there is no evidence linking GBS to the vaccine.