Search and filter adverse-event reports.
1,929,324 reports(865 ms)
arm soreness; general fatigue; not feeling well; This non-serious case was reported by a consumer via sales rep and described the occurrence of pain in arm in a 50-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown d…
swelling on face; This non-serious case was reported by a consumer via call center representative and described the occurrence of facial swelling in a 66-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the p…
received the first dose of the vaccine shingrix in my gluteus; This non-serious case was reported by a consumer via call center representative and described the occurrence of vaccine administered at inappropriate site in a patient who received Herpes zoster (S…
The first shot made me so sick; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of sickness in a patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient receiv…
slight reaction (fatigue) to Shingrix vaccine; This non-serious case was reported by a consumer and described the occurrence of fatigue in a patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Covid-19 vac…
Wrong age; This non-serious case was reported by a other health professional via call center representative and described the occurrence of inappropriate age at vaccine administration in a 24-year-old female patient who received DTPa (Infanrix) (batch number 4…
Pediarix expired dose administration; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 4-year-old female patient who received DTPa-HBV-IPV (Pediarix) (bat…
Do they need to revaccinate/restart the vaccination schedule; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of incomplete course of vaccination in a patient who did not receive Herpes zoster (Shi…
inappropriate schedule of vaccine/never received a second dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of incomplete course of vaccination in a elderly male patient who rece…
Shingles case after 1st dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of shingles in a female patient who received Herpes zoster (Shingrix) for prophylaxis. On 18-AUG-2025,…
Expire dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 14-month-old female patient who received MMR (Priorix) (batch number je9tp, expiry date 01-S…
fever with 100.4; Chills; This spontaneous case was reported by a physician and describes the occurrence of PYREXIA (fever with 100.4) and CHILLS (Chills) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 020F21A and 0…
Nausea; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (Nausea) in a male patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported.…
strong backache; chills; nausea; This spontaneous case was reported by a consumer and describes the occurrence of BACK PAIN (strong backache), CHILLS (chills) and NAUSEA (nausea) in a 62-year-old female patient who received SPIKEVAX NOS (SPIKEVAX NOS) for COVI…
autoimmune disease, rheumatoid arthritis/ joint pain/swelling in her legs and feet and could hardly lift her arms; autoimmune disease; her head felt like concrete (second dose); felt dizzy (second dose); bad stomach pains; old surgical scars (from surgical rem…
This is giving me full schizophrenia.; hearing beeping and hissing in ears; The initial case was missing the following minimum criteria: unspecified adverse event. Upon receipt of follow-up information on 02Sep2025, this case now contains all required informat…
Ministroke; Series of mini strokes; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 74-year-old female patient received BNT162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 27Sep2023 as dose 1 (toppac); single (Lot nu…
stomach ache; redness spreading down arm; Swollen arm; nausea; pain in arm at site and down arm; pain in arm at site and down arm; lump; redness at injection site; loss of appetite; low grade fever; chills; tired; lethargic; back ache; This is a spontaneous re…
reported being bedridden and having her limbs stiffen making it difficult to move; This is a spontaneous report received from a Consumer or other non HCP. A female patient (unknown if pregnant) received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)),…
had affected nervous system; breakout; normally gets allergies at end of the year; This is a spontaneous report received from a Consumer or other non HCP from License Party. Other Case identifier(s): AE-020617 (BIONTECH). A 53-year-old male patient received B…