Below is information from the manufacturer's inserts for the H1N1 vaccine, which can be found on the package inserts from each company for the vaccines. The links for these package inserts are listed as well.
All manufactured H1N1 vaccines contain thimerosal (ethyl mercury) except the LiveNasal spray manufactured by Medimune, “the safety and effectiveness of which have not been studied in pregnant or nursing mothers”.
All of the vaccine manufacturer’s inserts state that:
“Animal reproduction studies have not been conducted with [the vaccine]. It is also not known whether [the vaccine] can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. [The vaccine] should be given to a pregnant woman only if clearly needed.”
Sanofi Pasteur Vaccine
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/Approv...
The Sanofi Pasteur vaccine contains formaldehyde.
“Safety and effectiveness of [the vaccine] have not been established in pregnant women or nursing mothers or children <6 months of age.”
Note that the “immune response and safety of Fluzone vaccine was evaluated in 31 children between the ages of 6-26 months.”
Novartis Vaccines
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/Approv...
“Safety and effectiveness of [the vaccine] have not been established in pregnant women, nursing mothers or children less than 4 years of age.”
CSL Biotherapies
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/Approv...
“Safety and effectiveness of [the vaccine] have not been established in pregnant women, nursing mothers or in persons less than 18 years of age.”
“Neither Influenza A (H1N1) 2009 Monovalent Vaccine nor AFLURIA has been evaluated in children. Safety and effectiveness in the pediatric population have not been established.”
“Neither Influenza A (H1N1) 2009 Monovalent Vaccine nor AFLURIA has been evaluated for carcinogenic or mutagenic potential or for impairment of fertility.”
Medimmune, LLC (Live Nasal)
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/Approv...
“Safety and effectiveness of Influenza A (H1N1) 2009 Monovalent Vaccine Live, Intranasal have not been studied in pregnant women or nursing mothers.”
“It is not known whether [the vaccine] can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.”
“Do not administer [the vaccine] to children <24 months of age because of increased risk of hospitalization and wheezing.”
Note: the Sanofi Pasteur H1N1 (injectable) vaccine is the one that is recommended by the manufacturer for children ages 6 months and up. You will note the insert states that the "immune response and safety of Fluzone vaccine was evaluated in 31 children between the ages of 6-26 months.”
The immune response and safety of the four vaccines were evaluated in only a few hundred children and adults for only 1-3 weeks prior to the release of the vaccines for public use. [Source:
www.NVIC.org,
http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMa...]
These studies are not published in the vaccine inserts because the studies had not been completed at the time the inserts were compiled. This is why the only information in the inserts regarding use of the vaccine for "specific populations" is for the H1N1 vaccine's seasonal influenza likeness. In the case of the Sanofi Pasteur H1N1 vaccine it is the Fluzone seasonal influenza vaccine, which is made by the same process as the H1N1 vaccine.