Reporte zur Charge FH8U30

Symptomtext

Difficulty walking. Her legs were not working; Runny nose; Pfizer Covid Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Nov2021 14:30 (Lot number: FH8U30) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "injury to her tail bone", start date: 2005 (unspecified if ongoing); "Schizophrenia" (unspecified if ongoing). Concomitant medication(s) included: ARISTADA taken for schizophrenia (ongoing). Vaccination history included: Bnt162b2 (Dose 2, Lot number: EW0161, had no problems with the two vaccines), administration date: 29Apr2021, when the patient was 58 years old, for Covid-19 immunization, reaction(s): "had no problems with the two vaccines"; Bnt162b2 (Dose 1, Lot number: EW0153, had no problems with the two vaccines), administration date: 06Apr2021, when the patient was 58 years old, for Covid-19 immunization, reaction(s): "had no problems with the two vaccines". The following information was reported: IMMUNISATION (non-serious) with onset 24Nov2021 14:30, outcome "unknown", described as "Pfizer Covid Booster"; RHINORRHOEA (non-serious) with onset 25Nov2021, outcome "recovered" (26Nov2021), described as "Runny nose"; GAIT DISTURBANCE (non-serious) with onset 27Nov2021, outcome "not recovered", described as "Difficulty walking. Her legs were not working". The event "difficulty walking. her legs were not working" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rhinorrhoea. Additional information: Concomitant Products Aristada the last shot she received was 15Oct2021. She saw the doctor on Tuesday 30Nov2021 because her legs were not working. The runny nose was from Thursday 25Nov2021, Friday 26Nov2021. She took over the counter medication, Coriciden HP, it has runny nose on the label. Investigations: Went to the doctor's office Tuesday 30Nov2021. When went to doctor's office they were unsure if event was from covid vaccine or from previous injuries. She had x-rays that day, but had no results to provide. Additional Vaccines Administered on Same Date of the Pfizer Suspect: None. Adverse Event (AE) Details: Provide the time of onset of AE(s): Adverse Event: Runny nose, Time of Onset: (24-hour clock): In the evening about 4-5'clock. Adverse Event: Difficulty Walking, Time of Onset: (24-hour clock): When got out of bed in the morning. Did any AE(s) require a visit to: Emergency Room? No, Physician Office? Yes, because of difficulty walking, legs not working. Prior Vaccinations (within 4 weeks): None. AE(s) following prior vaccinations: None. Patient's Medical History (including any illness at time of vaccination)? None. At end of call, caller commented and requested if we find out if any issues or if anyone had side effects related to this lot number could we let her doctor know. No follow-up attempts are possible. No further information is expected.