CANRENONE for Product administration error: Side Effects & Safety Data
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There are 5 adverse event reports in the FDA FAERS database where CANRENONE was used for Product administration error.
Most Reported Side Effects for CANRENONE
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Hyperkalaemia | 68 | 23.8% | 0 | 50 |
| Hyponatraemia | 35 | 12.2% | 0 | 29 |
| Hypotension | 33 | 11.5% | 0 | 29 |
| Sopor | 25 | 8.7% | 0 | 25 |
| Dehydration | 24 | 8.4% | 0 | 23 |
| Syncope | 23 | 8.0% | 0 | 13 |
| Drug interaction | 21 | 7.3% | 0 | 16 |
| Bradycardia | 19 | 6.6% | 0 | 19 |
| Drug ineffective | 19 | 6.6% | 1 | 11 |
| Renal failure | 19 | 6.6% | 0 | 17 |
| Asthenia | 18 | 6.3% | 0 | 15 |
| Off label use | 18 | 6.3% | 10 | 15 |
| Acute kidney injury | 17 | 5.9% | 0 | 16 |
| Vomiting | 17 | 5.9% | 0 | 16 |
| Drug abuse | 16 | 5.6% | 0 | 16 |
Other Indications for CANRENONE
Hypertension (81)
Product used for unknown indication (78)
Cardiac failure (28)
Covid-19 (9)
Cardiovascular disorder (8)
Intentional self-injury (8)
Oedema (6)
Drug abuse (5)
Other Drugs Used for Product administration error
ACETAMINOPHEN (75)
CLOZAPINE (70)
QUETIAPINE (35)
VALPROATE (32)
DIAZEPAM (30)
ALPRAZOLAM (24)
VENLAFAXINE (24)
OXAZEPAM (23)
TRIHEXYPHENIDYL (23)
RISPERIDONE (22)