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A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

1,929,324 reports(834 ms)

#2837329Apr 22, 2025
Unknown·Age unknown·VA·HPV9

consumer received 3 doses of GARDASIL-9 at 8 years old, 8 years and 6 months old, and 9 year and 7 months old.; No additional AE reported; d 3 doses of GARDASIL-9 at 8 years old, 8 years and 6 months old, and 9 year and 7 months old; d 3 doses of GARDASIL-9 a…

No adverse eventProduct administered to patient of inappropriate age
#2837330Apr 22, 2025
Unknown·Age unknown·TX·VARCEL

No additional AE/PQC; HCP called and reported inadvertent administration of expired VARIVAX to a patient.; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. Limited patient demographics were provid…

Expired product administeredNo adverse event
#2837332Apr 22, 2025
Unknown·Age unknown·RV5

HCP reported that patient was administered the 1st and 2nd dose of ROTATEQ, but has not yet been administered the 3rd dose; No additional AE; This spontaneous report was received from a nurse and refers to a patient of unknown gender, 34-weeks-old at the time…

Inappropriate schedule of product administrationNo adverse event
#2837333Apr 22, 2025
Unknown·3 yrs·NY·VARCEL

No additional AE /PQC reported; HCP calling to report T/E; Information has been received from Business Partner/CRO on 10-Apr-2025. This spontaneous report was received from a Nurse and refers to a 3-year-old patient of unknown gender. The patient's medical h…

No adverse eventProduct storage error
#2837334Apr 22, 2025
Unknown·Age unknown·MO·VARCEL

Patient involved has not reported any medical concerns or symptoms/ No additional AE/PQC.; Expired dose of VARIVAX that was administered; This spontaneous report was received from a medical assistant, regarding a patient of unknown age and gender. The patient'…

Expired product administeredNo adverse event
#2837335Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication: The patie…

Drug interactionInappropriate schedule of product administration
#2837336Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837337Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interaction
#2837338Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837339Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837340Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837341Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837342Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837343Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837344Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication The patient…

Drug interactionInappropriate schedule of product administration
#2837345Apr 22, 2025
Unknown·Age unknown·MD·HEP

Drug Interaction with Burton tyrosine kinase inhibitors (BTKi's); HEPLISAV-B given at 0 and 3 months; Median anti-HBS titer was 0.05 mIU/mL with BTKi treatment; Initial report received on 21-Mar-2025. This report was retrieved from a publication. The patient…

Drug interactionInappropriate schedule of product administration
#2837346Apr 22, 2025
Male·Age unknown·FL·VARZOS

never received the second dose; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a male patient who received Herpes zoster (Shingrix) for prophylaxis. Previous…

Incorrect dose administered
#2837347Apr 22, 2025
Female·Age unknown·MEN

Arm was really sore; This non-serious case was reported by a other health professional via sales rep and described the occurrence of pain in arm in a 25-year-old female patient who received Men B NVS (Meningococcal B vaccine) for prophylaxis. On an unknown d…

Pain in extremity
#2837348Apr 22, 2025
Female·Age unknown·TX·VARZOS

received third dose of Shingrix; 2nd dose administered on 31 January 2025; This non-serious case was reported by a other health professional via sales rep and described the occurrence of extra dose administered in a 56-year-old female patient who received Herp…

Extra dose administeredInappropriate schedule of product administration
#2837349Apr 22, 2025
Female·64 yrs·NY·VARZOS

patient received the first dose of SHINGRIX 29 DEC 2022 and the second dose of SHINGRIX 11 APR 2025; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of drug dose administration interval too long in…

Inappropriate schedule of product administration
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