Reporte zur Charge LU6922AA

Symptomtext

feels like a cramp; fell and broke her left arm; stiffness that comes and goes and rotates from her right arm, shoulders, hips, legs and feet; pain; fell and broke her left arm; Initial information regarding an unsolicited valid non-serious case was received from a consumer/non-health care professional via Medical Information (Reference number- 00792710) and transmitted to Sanofi on 30-Sep-2021. This case involves a 65 years old female patient who fell (fall) and broke her left arm (upper limb fracture), feels like a cramp (muscle spasms), pain and stiffness (musculoskeletal stiffness), while received vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. Medical history, concomitant medication, past medical treatment, vaccination and family history were not provided. Patient had ongoing metal allergy like cobalt, thimerosal and knows it was probably the aluminum and 2-phenoxethanol that is causing her the issues with the vaccine. On an unknown date, the patient received a 0.5 mL dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [oral solution, lot number: LU6922AA, expiry date: 22-Jan-2023], via an intramuscular route in right deltoid for prophylactic vaccination. On 26-Sep-2021, the patient fell (fall) and broke her left arm (upper limb fracture) and went to the emergency room (suggested that she had the vaccine), pain and stiffness (musculoskeletal stiffness) that comes and goes and rotates from her right arm, shoulders, hips, legs and feet bu she wouldn't know about her left arm since it is casted and broken same day following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. On an unknown date the patient developed a non-serious doesn't have cramps but feels like a cramp (muscle spasms) (unknown latency) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. It was reported ''Paperwork states Adacel doesn't have a preservative but the list is incorrect because those are preservatives.'' Other relevant laboratory test were not provided. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the patient was recovering from all the reported events.