Parsabiv: adverse event reports filed with FDA

2,190

reports as suspect product

0% of all reports · about 233 a year

14

reports, 12 months to June 2026

30 in the 12 months before

33.9%

marked serious by the reporter

35.7% across the class

9.2%

record death among outcomes, as reported

201 reports · not verified by FDA

Reports by month, five years

Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.

By year received

2026 covers reports received through June 2026 only.

Reactions recorded in the reports

share of Parsabiv reports recording the termmedian drug in calcium-sensing receptor agonist

1. Underdoseless than the intended dose10.6%233
2. Nauseafeeling sick7.9%174
3. Product storage errorthe product was stored wrongly6.7%147
4. Blood parathyroid hormone increased6.3%138
5. Blood calcium decreased5.2%113
6. Hypocalcaemialow blood calcium4.9%108
7. Diarrhoealoose or frequent stools4.4%97
8. Vomitingbeing sick3.9%86
9. Circumstance or information capable of leading to medication errora situation that could lead to a medication error3.7%82
10. Drug ineffectivethe medicine did not work as expected2.6%57
11. Therapy non-responderthe treatment did not work2.6%56
12. Pruritusitching2.3%51
13. Deaththe patient died; cause not stated by this term2.3%50
14. Headachehead pain2%43
15. Abdominal discomfortstomach discomfort1.8%40
16. Off label useused for a purpose or in a way not on the label1.8%40
17. Gastrointestinal disorder1.8%39
18. Drug intolerancethe medicine was not tolerated1.7%38
19. Dizzinesslight-headedness or unsteadiness1.6%35
20. Muscle spasmsmuscle cramps1.6%35
21. Cardiac failureheart failure1.6%34
22. Shunt stenosis1.4%31
23. Blood calcium increased1.4%30
24. Paraesthesiatingling or pins and needles1.4%30
25. Blood parathyroid hormone abnormal1.3%29
26. Rashskin rash1.3%28
27. Arthralgiajoint pain1.2%27
28. Malaisegeneral feeling of being unwell1.2%26
29. Gastrointestinal haemorrhagebleeding in the stomach or bowel1.1%25
30. Pneumonialung infection1.1%25

Top 30 of 249 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the median share across the 5 drugs in the calcium-sensing receptor agonist class; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

Outcomes recorded

Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 47,026 reports in the class. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."

Patients and reporters

Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 79.3% of reports give the United States as the country of the event or reporter.

Reason for use recorded

The indication field is filled in by the reporter and is often blank; shares are of all 2,190 reports.

Drugs most often listed in the same reports

Other products listed in reports where Parsabiv is a suspect product, whatever their own role. Co-listing means the two were recorded together; it says nothing about either product's part in the event. Only the 2,500 most-reported names are counted here.

In context

Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

Other drugs in the calcium-sensing receptor agonist class

Ordered by report count for navigation only. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic." A brand and its generic are separate rows because reporters name them separately.

Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Parsabiv as a suspect or interacting product; reports listing it only as a concomitant medication (83) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.