🇺🇸 Palbociclib PD-0332991 in United States
47 US adverse-event reports
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
- Window: 23 April 2025 – 23 April 2026
- Total reports: 47
Most-reported reactions
- Asthenia — 6 reports (12.77%)
- Confusional State — 5 reports (10.64%)
- Nausea — 5 reports (10.64%)
- Neutrophil Count Decreased — 5 reports (10.64%)
- Pleural Effusion — 5 reports (10.64%)
- Pneumonia — 5 reports (10.64%)
- Acute Kidney Injury — 4 reports (8.51%)
- Dyspnoea — 4 reports (8.51%)
- Failure To Thrive — 4 reports (8.51%)
- Fall — 4 reports (8.51%)
Other Oncology approved in United States
Frequently asked questions
Is Palbociclib PD-0332991 approved in United States?
Palbociclib PD-0332991 does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Palbociclib PD-0332991 in United States?
GBG Forschungs GmbH is the originator. The local marketing authorisation holder may differ — check the official source linked above.