Vaccines on the CDC’s Pediatric Recommended Schedule

FDA labelling law requires vaccine manufacturers to include on their product inserts:

“Adverse reactions. This section must describe the overall adverse reaction profile of the drug based on the entire safety database. For purposes of prescription drug labeling, an adverse reaction is an undesirable effect, reasonably associated with use of a drug, that may occur as part of the pharmacological action of the drug or may be unpredictable in its occurrence. This definition does not include all adverse events observed during use of a drug, only those adverse events for which there is some basis to believe there is a causal relationship between the drug and the occurrence of the adverse event.” (emphasis added)

For the most recent product inserts on vaccines currently licensed in the U.S., visit the FDA Page.

DTaP & Tdap (diphtheria, tetanus, acellular pertussis)

Hib (Haemophilus influenza type b)

Hepatitis A

Hepatitis B

HPV (human papillomavirus)

Influenza

IPV (inactivated poliovirus)

Meningococcal

MMR (measles, mumps, rubella)

PCV 13 (pneumococcal conjugate)

PPSV23 (pneumococcal polysaccharide)

Rotavirus

Varicella (chickenpox)

Vaccines on the CDC’s Adult Recommended Schedule

All of the above plus:

Zoster (shingles)

 

 

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