Reporte zur Charge EW0169 (EW969)

Symptomtext

At times it was Throbbing to Pain level 10; Swollen fingers, hands/Swollen feet; Swollen wrists/Swollen ankles; Pain in Shoulders, Hips; Could not walk for several weeks; Loss of Bladder control; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 21Apr2021 08:30 (Lot Number: EW0169 (EW969)) at age of 71-year-old as dose 2, single for COVID-19 immunisation. The patient is not pregnant at the time of the vaccination. Medical history included seasonal allergy. Concomitant medications included atorvastatin calcium (LIPITOR); fexofenadine hydrochloride (ALLEGRA); hydrochlorothiazide; multivitamin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took potassium chloride (KDUR) and experienced allergy, took bnt162b2 dose 1 on 01Apr2021 08:30 am (lot number=EL3302) in left arm at age of 71-year-old for COVID-19 immunisation. On 25Apr2021 16:00, the patient experienced swollen fingers, hands, (At times it was Throbbing to Pain level 10) wrists ,feet, ankles, pain in shoulders, hips, the patient could not walk for several weeks, lost of bladder control. The events resulted in doctor or other healthcare professional office/clinic visit. The case was reported as non-serious. The patient received treatment for the events included medication and pain medication. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the events was resolving.