DYDROGESTERONE for Luteal phase deficiency: Side Effects & Safety Data
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There are 12 adverse event reports in the FDA FAERS database where DYDROGESTERONE was used for Luteal phase deficiency.
Most Reported Side Effects for DYDROGESTERONE
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Maternal exposure during pregnancy | 117 | 34.4% | 2 | 8 |
| Abortion spontaneous | 93 | 27.4% | 0 | 0 |
| Ovarian hyperstimulation syndrome | 34 | 10.0% | 0 | 28 |
| Foetal exposure during pregnancy | 27 | 7.9% | 2 | 1 |
| Exposure during pregnancy | 20 | 5.9% | 0 | 6 |
| Off label use | 18 | 5.3% | 0 | 13 |
| Meningioma | 17 | 5.0% | 0 | 9 |
| Premature baby | 16 | 4.7% | 1 | 1 |
| Product use in unapproved indication | 15 | 4.4% | 0 | 8 |
| Toxicity to various agents | 11 | 3.2% | 0 | 0 |
| Vaginal haemorrhage | 11 | 3.2% | 0 | 10 |
| Ascites | 10 | 2.9% | 0 | 7 |
| Headache | 10 | 2.9% | 0 | 0 |
| Intentional self-injury | 10 | 2.9% | 0 | 0 |
| Low birth weight baby | 10 | 2.9% | 0 | 1 |
Other Indications for DYDROGESTERONE
Hormone replacement therapy (99)
Product used for unknown indication (48)
Assisted reproductive technology (26)
In vitro fertilisation (26)
Foetal exposure during pregnancy (9)
Intentional self-injury (8)
Infertility (6)
Abortion spontaneous (5)
Amenorrhoea (5)
Assisted fertilisation (5)