Fetal Death

Adverse event reports after tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccines in pregnant women.

“The most frequent pregnancy-specific AE was spontaneous abortion in 22 (16.7%) reports.”

#Fetal #Death #Pregnancy #Tdap #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/22727350/

Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season?

#Fetal #Death #Pregnancy #Flu #Influenza #H1N1 #Vaccines #VAERS #MedScienceResearch

http://www.ncbi.nlm.nih.gov/pubmed/23023030

Elective termination of pregnancy after vaccination reported to the Vaccine Adverse Event Reporting System (VAERS): 1990-2006.

#Pregnancy #Fetal #Death
#VAERS #Vaccine #Abortion #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/18406499/

Surveillance of Adverse Events After Seasonal Influenza Vaccination in Pregnant Women and Their Infants in the Vaccine Adverse Event Reporting System, July 2010-May 2016.

“Among IIV reports, the most frequent pregnancy-specific AE was spontaneous abortion in 62 (11.4%) reports, followed by stillbirth in ten (1.8%) and preterm delivery in six (1.1%).”

#Fetal #Death #Pregnancy #Flu #Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/27988883/

? [Vaccines, biotechnology and their connection with induced abortion].

“Diploid cells (WI-38, MRC-5) vaccines have their origin in induced abortions. Among these vaccines we fi nd the following: rubella, measles, mumps, rabies, polio, smallpox, hepatitis A, chickenpox, and herpes zoster. Nowadays, other abortion tainted vaccines cultivated on transformed cells (293, PER.C6) are in the pipeline: flu, Respiratory Syncytial and parainfluenza viruses, HIV, West Nile virus, Ebola, Marburg and Lassa, hepatitis B and C, foot and mouth disease, Japanese encephalitis, dengue, tuberculosis, anthrax, plague, tetanus and malaria. The same method is used for the production of monoclonal antibodies and other proteins, gene therapy and genomics. Technology enables us to develop the aforementioned products without resorting to induced abortion. Full disclosure of the cell origin in the labelling of vaccines and other products must be supported. There are vaccines from non-objectionable sources which should be made available to the public. When no alternative vaccines exist, ethical research must be promoted. Non-objectionable sources in the production of monoclonal antibodies, gene therapy and genomics must be encouraged. It is not be consistent to abstain from products originated in embryonic stem cells and at the same time approve of products obtained from induced abortions. It is of paramount importance to avoid that induced abortion technology seeps into every field of Medicine.”

#Abortion #Aborted #Fetal #Cells #MMR #Rubella #Measles #Mumps #Rabies #Polio #Smallpox #Hepatitis A #Chickenpox #Herpes #Zoster #Shingles
#Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/18611078/

Vaccines originating in abortion.

Furton EJ. Ethics Medics. 1999.
PMID 11657845

#Aborted #Fetal #Tissue
#Vaccines #Rubella #Abortion #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/11657845/

Full text:

http://www.immunize.org/concerns/furton.pdf

Yellow fever vaccination during pregnancy and spontaneous abortion: a case-control study.

#Pregnancy #Abortion
#Fetal #Death #Yellow #Fever
#Vaccine #MedScienceResearch

https://www.ncbi.nlm.nih.gov/m/pubmed/9484965/