Loratadine

Common brands: Claritin Reditabs, Claritin Liqui-Gels, Claritin Allergy, Claritin, Allergy Relief

Top reporter: Bayer Healthcare Llc.

Nonsteroidal Anti-inflammatory Drug [EPC]Corticosteroid [EPC]Provitamin D2 Compound [EPC]Proton Pump Inhibitor [EPC]Benzodiazepine [EPC]
105,876
Total Reports
30,960
Serious Reports
4,599
Death Reports
30
Reported Reactions
Death Report Ratio: Moderate (4.34%)

Patient Demographics

Male
32,525
Female
63,888

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Loratadine.

# Reaction Reports % of Total
1 DRUG INEFFECTIVE 13,016
12.3%
2 FATIGUE 6,535
6.2%
3 NAUSEA 5,789
5.5%
4 HEADACHE 5,278
5.0%
5 DIARRHOEA 4,752
4.5%
6 DYSPNOEA 4,732
4.5%
7 OFF LABEL USE 4,568
4.3%
8 DIZZINESS 4,297
4.1%
9 PAIN 4,041
3.8%
10 RASH 3,391
3.2%
11 PRURITUS 3,264
3.1%
12 COUGH 3,015
2.8%
13 VOMITING 2,973
2.8%
14 SOMNOLENCE 2,945
2.8%
15 ARTHRALGIA 2,819
2.7%
16 ASTHENIA 2,709
2.6%
17 PNEUMONIA 2,682
2.5%
18 ANXIETY 2,671
2.5%
19 MALAISE 2,626
2.5%
20 INSOMNIA 2,589
2.4%
21 PYREXIA 2,328
2.2%
22 FALL 2,313
2.2%
23 PAIN IN EXTREMITY 2,242
2.1%
24 FEELING ABNORMAL 2,107
2.0%
25 URTICARIA 2,094
2.0%
26 PRODUCT USE ISSUE 2,088
2.0%
27 DEPRESSION 2,072
2.0%
28 BACK PAIN 2,023
1.9%
29 WEIGHT DECREASED 1,988
1.9%
30 CONDITION AGGRAVATED 1,916
1.8%

Important Disclaimer

FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.