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              ANAPHYLAXIES AFTER EXPOSURE TO COVID-19 VACCINES:
              A CASE SERIES

              F. CHAHED, J. REBAI, H. BEN ROMDHANE, A. CHAABENE, K. AOUAM, N. BEN FREDJ, N.
              BEN FADHEL
              DEPARTMENT OF CLINICAL PHARMACOLOGY. FACULTY OF MEDICINE OF MONASTIR. UNIVERSITY
              OF MONASTIR. TUNISIA


              BACKGROUND: Vaccines against Covid-19 were recognized as one of the important
              public health interventions to control the pandemic. Vaccines are supposed to supply
              active immunity to unique antigens. Hypersensitivity reactions to Covid-19 vaccines
              have been reported since  the initiation of the vaccination campaigns. Severe
              Anaphylaxis has been rarely described.

              OBJECTIVE:  To evaluate the particularities of severe anaphylaxis (grade III) after
              exposure to covid-19 vaccine.
              METHODS: We included all cases of severe anaphylaxis (grade III according to Ring
              and Messmer Ring and Messmer Anaphylaxis Grading Scale) after Covid 19 vaccine
              intake; notified  to the Pharmacovigilance Unit of the Clinical Pharmacology
              Department of the University Hospital of Monastir (Tunisia) between March 2020 and
              January 2022. An allergy work up to suspected vaccines (skin tests to vaccines and
              excipients; drug provocation test  to polyethylene glycol) was performed. The
              causative relationship between the hypersensitivity reaction and the vaccine
              administration was established according to the probability scale of adverse drug
              reactions published by Naranjo et al.

              RESULTS: Six patients (4F/2M) were included in this study. The median age was 42
              years (IQR: 27-72 years).  Underlying atopy was presented in three patients. The
              suspected Covid-19 vaccine was as follows: the mRNA vaccine (BNT162b2 (n= 3), and
              inactivated virus vaccines (SinoVac: n= 2) and  CoronaVac: n=1). The median time
              interval between vaccination and the onset of anaphylactic reaction was 10 minutes
              (2min- 12 hours). The offended dose was the first one in all patients. Four patients
              agreed to undergo allergy work up. Skin tests were positive to only  one patient
              (Sinovac vaccine). Oral provocation test to the excipient (PEG) was performed in two
              patients and revealed negatives.
              Of all patients, none had the  second booster dose  to the offended vaccines.
              Moreover, all patients refuse vaccination with another Covid-19 vaccine

              CONCLUSIONS: Additional data are needed to evaluate the value of allergy work up
              in the investigation of COVID-19 vaccine hypersensitivity.

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