Product name as reported
Shower To Shower Talcum Product: adverse event reports filed with FDA
313 reports list it as a suspect or interacting product, 2014–2016.
- 313
- reports as suspect product
- 0% of all reports · about 26 a year
- 0
- reports, 12 months to June 2026
- 0 in the 12 months before
- 100%
- marked serious by the reporter
- 57.4% across all reports
- 11.2%
- record death among outcomes, as reported
- 35 reports · not verified by FDA
Between May 2014 and December 2016, 313 adverse event reports received by FDA list the product name "Shower To Shower Talcum Product" as reporters wrote it as a suspect or interacting product. Reports that mention it only as a concomitant medication (0) are left out of every figure here.
In the 12 months to June 2026, 0 reports listed it, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 26 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
Reporters most often recorded ovarian cancer (86.3%), ovarian cancer stage III (8%) and ovarian cancer stage I (2.6%). A report can list several reactions, so shares add to more than 100%; 22 different terms appear across these reports. Ovarian cancer is recorded in 86.3% of these reports, against 0% of all reports in the database.
100% of the reports are marked serious by the reporter; 11.2% record death among the outcomes and 7.3% record hospitalisation, as reported. 64.2% of the reports came from other health professionals, and the largest patient age group is 45 to 64 (18.8%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
No report listing Shower To Shower Talcum Product was received in the five years to June 2026; the latest was received in December 2016.
By year received
Reactions recorded in the reports
share of Shower To Shower Talcum Product reports recording the termall reports in the database
- Ovarian cancer86.3%270
- Ovarian cancer stage III8%25
- Ovarian cancer stage I2.6%8
- Ovarian cancer stage IV2.2%7
- Ovarian cancer stage II1.6%5
- Ovarian cancer metastatic1%3
- Anaemialow red blood cells0.3%1
- Cervicitis cystic0.3%1
- Cervix carcinoma0.3%1
- Cervix carcinoma stage IV0.3%1
- Chronic kidney diseaselong-term kidney disease0.3%1
- Coagulopathy0.3%1
- Endometrial adenocarcinoma0.3%1
- Fallopian tube cancer stage III0.3%1
- Fatiguetiredness0.3%1
- Gastric ulcera stomach ulcer0.3%1
- Gastritisinflamed stomach lining0.3%1
- Gastrointestinal haemorrhagebleeding in the stomach or bowel0.3%1
- Hypernatraemia0.3%1
- Hypokalaemialow blood potassium0.3%1
- Invasive ductal breast carcinoma0.3%1
- Lactic acidosisa build-up of lactic acid in the blood0.3%1
Top 22 of 22 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 share of all reports in the database; 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 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 100% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Therapeutic skin care topical | 8 | 2.6% |
| Prophylaxis | 3 | 1% |
The indication field is filled in by the reporter and is often blank; shares are of all 313 reports.
In context
| Measure | Shower To Shower Talcum Product | All reports |
|---|---|---|
| Reports as suspect product | 313 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 0 | 1,332,454 |
| Marked serious | 100% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 112 | 91 |
| Hospitalisation recorded, per 1,000 reports | 73 | 213 |
| Consumer-filed share | 34.2% | 45.8% |
| Top term, share of reports | Ovarian cancer 86.3% | 0% |
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."
Questions about Shower To Shower Talcum Product reports
How many adverse event reports has FDA received for Shower To Shower Talcum Product?
313 reports list Shower To Shower Talcum Product as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 0 of them arrived in the latest 12 months. Another 0 list it only as a concomitant medication.
What reactions are recorded in Shower To Shower Talcum Product reports?
ovarian cancer (86.3%), ovarian cancer stage III (8%), ovarian cancer stage I (2.6%), ovarian cancer stage IV (2.2%) and ovarian cancer stage II (1.6%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Shower To Shower Talcum Product was responsible.
How serious are the reports?
100% are marked serious by the reporter. Among the outcomes recorded, 11.2% of reports include death and 7.3% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
lawyer (64.2%), consumer or non-health professional (34.2%) and not given (1.6%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Shower To Shower Talcum Product rising?
0 reports in the 12 months to June 2026, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Shower To Shower Talcum Product was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Shower To Shower Talcum Product?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
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 Shower To Shower Talcum Product as a suspect or interacting product; reports listing it only as a concomitant medication (0) 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.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.