RIFAXIMIN for Ammonia increased: Side Effects & Safety Data
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There are 156 adverse event reports in the FDA FAERS database where RIFAXIMIN was used for Ammonia increased.
Most Reported Side Effects for RIFAXIMIN
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Death | 3,687 | 26.6% | 3,682 | 303 |
| Hospitalisation | 1,605 | 11.6% | 198 | 1,602 |
| Therapy interrupted | 875 | 6.3% | 162 | 563 |
| Off label use | 802 | 5.8% | 46 | 115 |
| Diarrhoea | 709 | 5.1% | 46 | 167 |
| Ammonia increased | 676 | 4.9% | 90 | 564 |
| Inability to afford medication | 672 | 4.9% | 89 | 396 |
| Insurance issue | 577 | 4.2% | 88 | 336 |
| Confusional state | 530 | 3.8% | 53 | 344 |
| Hepatic cirrhosis | 480 | 3.5% | 305 | 224 |
| Hepatic encephalopathy | 462 | 3.3% | 93 | 347 |
| Product use in unapproved indication | 439 | 3.2% | 21 | 57 |
| Drug ineffective | 436 | 3.2% | 68 | 148 |
| Fall | 433 | 3.1% | 81 | 322 |
| Product use issue | 421 | 3.0% | 91 | 258 |
Other Indications for RIFAXIMIN
Product used for unknown indication (6,357)
Hepatic encephalopathy (2,587)
Hepatic cirrhosis (1,346)
Irritable bowel syndrome (964)
Gastrointestinal bacterial overgrowth (626)
Product use in unapproved indication (421)
Liver disorder (384)
Hepatic failure (361)
Diarrhoea (210)
Off label use (99)