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Drug Search by Year (Detail)

Side effect search by year (detail)

Drug:

Reaction: ACCIDENTAL EXPOSURE TO PRODUCT

20250101 - 20251231

No. 1 - 100

Next page: 2 next page>>
No.
safetyreportid
occurcountry
patientonsetage
patientsex 1:M 2:F
Adverse reaction
Drug (openfda.generic_name, medicinalproduct)
1
25491822
US
30 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
2
25491827
US
60 2
Limb injury, Accidental exposure to product, Device difficult to use, Injection site erythema, Injection site haemorrhage,
EVOLOCUMAB, EVOLOCUMAB,
3
25491871
US
85 2
Wrong technique in device usage process, Product dose omission issue, Accidental exposure to product,
BELIMUMAB,
4
25492309
GB
Device breakage, Accidental exposure to product,
5
25492320
US
1
Accidental exposure to product,
AZELASTINE HYDROCHLORIDE, AZELASTINE,
6
25492607
CN
Accidental exposure to product, Device leakage,
GUSELKUMAB,
7
25492855
US
2
Device defective, Incorrect dose administered by device, Needle issue, Accidental exposure to product,
METHOTREXATE, METHOTREXATE SODIUM, FOLIC ACID,
8
25493394
US
71 1
Road traffic accident, Device difficult to use, Accidental exposure to product, Drug dose omission by device, Product communication issue,
EVOLOCUMAB, EVOLOCUMAB, EVOLOCUMAB,
9
25493411
US
2
Incorrect dose administered, Accidental exposure to product, Product delivery mechanism issue,
AZELASTINE HYDROCHLORIDE, AZELASTINE,
10
25493514
US
2
Accidental exposure to product, Wrong technique in product usage process,
FLUTICASONE PROPIONATE AND SALMETEROL,
11
25493833
US
1
Device malfunction, Complication of device insertion, Accidental exposure to product, Device leakage, Drug dose omission by device,
OFATUMUMAB, LEVOTHYROXINE SODIUM,
12
25494150
US
2
Sensory disturbance, Injury associated with device, Wrong patient received product, Accidental exposure to product, Device use error, Injection site pain, Injection site swelling,
EVOLOCUMAB,
13
25494656
US
56 2
Exposure via skin contact, Injection site haemorrhage, Wrong technique in device usage process, Accidental exposure to product, Incorrect dose administered,
BELIMUMAB,
14
25494791
US
60 2
Accidental exposure to product, Product dose omission issue, Device issue,
GUSELKUMAB,
15
25495232
US
2
Device issue, Accidental exposure to product,
GUSELKUMAB,
16
25495566
US
83 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
17
25495598
US
58 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
18
25495703
US
50 2
Product use in unapproved indication, Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB,
19
25495704
US
61 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
20
25495708
US
76 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
21
25495727
US
70 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB,
22
25495784
US
1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB,
23
25495787
US
82 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
24
25495796
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
25
25495834
US
1
Accidental exposure to product, Exposure via skin contact,
SARILUMAB,
26
25495840
US
72 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
27
25496060
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
28
25490969
US
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
29
25491071
US
64 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
30
25491227
US
1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB,
31
25491369
US
60 1
Accidental exposure to product, Exposure via skin contact,
SARILUMAB,
32
25491452
CH
1
Device deployment issue, Accidental exposure to product, Product dose omission issue,
GOLIMUMAB,
33
25491489
US
13 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
34
25491616
US
12 2
Injection site discharge, Accidental exposure to product, Incorrect dose administered,
SOMATROPIN, SOMATROPIN,
35
25489953
US
61 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
36
25490022
US
54 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
37
25490153
US
61 2
Accidental exposure to product, Device difficult to use, Drug dose omission by device, Injection site pain,
ETANERCEPT,
38
25490273
US
27 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
39
25490274
US
76 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
40
25490280
US
17 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
41
25490287
US
75 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
42
25490361
US
52 2
Rash, Underdose, Injection site pain, Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
43
25490371
US
64 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
44
25486442
US
61 2
Ocular discomfort, Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
45
25486455
US
42 2
Device malfunction, Accidental exposure to product, Device leakage,
PEGFILGRASTIM, PEGFILGRASTIM,
46
25486479
US
74
Rash, Pruritus, Device difficult to use, Accidental exposure to product, Rubber sensitivity, Drug dose omission by device,
EVOLOCUMAB,
47
25486626
US
61 1
Injection site pain, Device difficult to use, Accidental exposure to product, Incorrect dose administered by device,
EVOLOCUMAB,
48
25486810
US
76
Needle issue, Accidental exposure to product, Incorrect dose administered,
USTEKINUMAB, USTEKINUMAB,
49
25487817
US
Product dose omission issue, Drug delivery system malfunction, Accidental exposure to product,
GOLIMUMAB,
50
25487828
US
71 1
Product dose omission issue, Needle issue, Accidental exposure to product,
GUSELKUMAB,
51
25489017
US
53 2
Eye irritation, Bacterial rhinitis, Eye discharge, Ocular discomfort, Product dose omission issue, Accidental exposure to product, Device defective, Device issue,
OMALIZUMAB, ETANERCEPT, ETANERCEPT, METHOTREXATE, METHOTREXATE SODIUM, METHOTREXATE, METHOTREXATE SODIUM, TIRZEPATIDE, ESCITALOPRAM, ESCITALOPRAM OXALATE, ESCITSLOPRAM, HYDROXYZINE,
52
25489128
US
13 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
53
25489135
US
74 1
Hypoacusis, Accidental exposure to product, Exposure via skin contact,
INSULIN GLARGINE,
54
25489137
US
81 1
Accidental exposure to product, Exposure via skin contact,
INSULIN GLARGINE AND LIXISENATIDE,
55
25489179
US
14 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
56
25489192
US
76 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
57
25489220
US
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
58
25489368
US
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
59
25489384
US
71 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
60
25489390
US
70 1
Product dispensing error, Accidental exposure to product, Exposure via skin contact,
INSULIN GLARGINE,
61
25489475
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
62
25489481
US
46 1
Accidental exposure to product, Exposure via skin contact, Off label use,
INSULIN GLARGINE,
63
25489497
US
7 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
64
25490504
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
65
25490570
US
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
66
25490781
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
67
25490804
US
67 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
68
25490829
US
9 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
69
25481256
US
2
Exposure via skin contact, Wrong technique in device usage process, Accidental exposure to product, Underdose, Product complaint,
BELIMUMAB,
70
25481352
US
29 1
Accidental exposure to product, Wrong technique in device usage process,
BELIMUMAB,
71
25481403
US
1
Needle issue, Accidental exposure to product, Drug dose omission by device,
72
25481681
US
70 1
Exposure via skin contact, Wrong technique in device usage process, Accidental exposure to product, Product dose omission issue,
MEPOLIZUMAB,
73
25481718
US
33 2
Injection site haemorrhage, Accidental exposure to product, Device malfunction,
FREMANEZUMAB-VFRM,
74
25481814
US
1
Accidental exposure to product, Injection site pain,
75
25482506
US
42 2
Product dose omission issue, Needle issue, Product complaint, Accidental exposure to product, Product closure issue, No adverse event,
OMALIZUMAB, OMALIZUMAB,
76
25482585
US
2
Accidental exposure to product, Accidental underdose, Device defective, No adverse event,
OMALIZUMAB,
77
25483101
US
1
Device malfunction, Needle issue, Accidental exposure to product,
OFATUMUMAB,
78
25483434
US
69 2
Injection site pain, Injection site bruising, Injection site haemorrhage, Device difficult to use, Accidental exposure to product, Drug dose omission by device,
EVOLOCUMAB,
79
25483764
US
76 1
Drug effect less than expected, Accidental exposure to product, Inappropriate schedule of product administration,
DICLOFENAC SODIUM,
80
25484008
US
2
Accidental exposure to product, Incorrect dose administered by device,
ESKETAMINE HYDROCHLORIDE, ESKETAMINE HYDROCHLORIDE, ESKETAMINE HYDROCHLORIDE,
81
25484118
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
82
25484238
US
19 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
83
25484297
US
13 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
84
25484357
US
65 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB,
85
25484373
US
2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
86
25484382
US
73 1
Accidental exposure to product, Exposure via skin contact, Incorrect dose administered,
DUPILUMAB,
87
25484415
US
75 1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
88
25484426
US
69 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
89
25484429
US
26 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
90
25484770
US
47 2
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
91
25485171
CA
53 2
Device deployment issue, Product dose omission issue, Accidental exposure to product,
GOLIMUMAB,
92
25485485
US
1
Injury associated with device, Accidental exposure to product, Device use error,
EVOLOCUMAB,
93
25486249
US
1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
94
25486286
US
51 2
Needle issue, Accidental exposure to product, Product dose omission issue,
GUSELKUMAB,
95
25486317
US
1
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB, DUPILUMAB, OCTOCRYLENE, AVOBENZONE, TRIAMCINOLONE ACETONIDE, TRIAMCINOLONE ACETONIDE OINTMENT USP, 0.05%, MOMETASONE FUROATE, MOMETASONE,
96
25475939
US
Accidental exposure to product, Exposure via skin contact,
DUPILUMAB,
97
25476095
US
2
Device issue, Injection site haemorrhage, Accidental exposure to product, Incorrect dose administered by device, Device leakage,
OFATUMUMAB,
98
25476422
US
47 2
Accidental exposure to product, Underdose,
GALCANEZUMAB-GNLM, EPINEPHRINE,
99
25477266
US
Accidental exposure to product,
OCTREOTIDE ACETATE, OCTREOTIDE ACETATE, OCTREOTIDE ACETATE,
100
25477366
US
2
Condition aggravated, Device leakage, Accidental exposure to product,

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Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.

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last_updated

2025-07-29

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