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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AMARANTHUS RETROFLEXUS POLLEN Cause Hypersensitivity? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Hypersensitivity have been filed in association with AMARANTHUS RETROFLEXUS POLLEN (S02 ALLER-TOTAL). This represents 6.3% of all adverse event reports for AMARANTHUS RETROFLEXUS POLLEN.

6
Reports of Hypersensitivity with AMARANTHUS RETROFLEXUS POLLEN
6.3%
of all AMARANTHUS RETROFLEXUS POLLEN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Hypersensitivity From AMARANTHUS RETROFLEXUS POLLEN?

Of the 6 reports.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMARANTHUS RETROFLEXUS POLLEN. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does AMARANTHUS RETROFLEXUS POLLEN Cause?

Anaphylactic reaction (26) Throat irritation (20) Cough (17) Urticaria (14) Pruritus (13) Throat tightness (11) Dyspnoea (10) Rhinorrhoea (10) Eye pruritus (9) Injection site reaction (9)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Related Pages

AMARANTHUS RETROFLEXUS POLLEN Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity AMARANTHUS RETROFLEXUS POLLEN Demographics