Drug:
Reaction: DRUG DOSE OMISSION BY DEVICE
20260101 - 20261231
No. 1001 - 1100
| No. | safetyreportid |
occurcountry |
patientonsetage |
patientsex 1:M 2:F |
|---|---|---|---|---|
Adverse reaction |
||||
Drug (openfda.generic_name, medicinalproduct) |
||||
| 1001 | 26356176 |
US |
2 | |
Drug dose omission by device, Device breakage, |
||||
SOMATROPIN, |
||||
| 1002 | 26356178 |
US |
1 | |
Drug dose omission by device, Wrong technique in device usage process, Device breakage, Device issue, |
||||
ALBUTEROL SULFATE, |
||||
| 1003 | 26356187 |
CO |
||
Drug dose omission by device, Device issue, |
||||
SOMATROPIN, |
||||
| 1004 | 26356359 |
US |
68 | 2 |
Device leakage, Accidental exposure to product, Needle issue, Drug dose omission by device, |
||||
SECUKINUMAB, |
||||
| 1005 | 26344248 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1006 | 26345303 |
US |
1 | |
Drug dose omission by device, Device difficult to use, Needle issue, |
||||
SOMATROPIN, |
||||
| 1007 | 26345523 |
US |
82 | |
Wrong technique in product usage process, Drug dose omission by device, No adverse event, |
||||
ALBUTEROL SULFATE, |
||||
| 1008 | 26345526 |
US |
65 | 2 |
Drug dose omission by device, |
||||
EVOLOCUMAB, |
||||
| 1009 | 26345529 |
US |
||
Drug dose omission by device, Device delivery system issue, Off label use, Wrong technique in product usage process, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1010 | 26345707 |
US |
27 | |
Drug dose omission by device, Device delivery system issue, No adverse event, |
||||
LEVALBUTEROL TARTRATE, LEVALBUTEROL TARTRATE, MONTELUKAST, |
||||
| 1011 | 26345802 |
US |
29 | |
Drug dose omission by device, Device defective, No adverse event, |
||||
RISPERIDONE, |
||||
| 1012 | 26346114 |
US |
50 | |
Drug dose omission by device, Device delivery system issue, Device malfunction, No adverse event, |
||||
ALBUTEROL SULFATE, ALBUTEROL SULFATE, |
||||
| 1013 | 26346158 |
US |
||
Drug dose omission by device, Device mechanical issue, |
||||
GLATIRAMER ACETATE, GLATIRAMER ACETATE, |
||||
| 1014 | 26346438 |
KR |
7 | 2 |
Drug dose omission by device, Device mechanical issue, Device power source issue, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1015 | 26346443 |
US |
2 | |
Drug dose omission by device, Device breakage, |
||||
SOMATROPIN, |
||||
| 1016 | 26346461 |
KR |
10 | 2 |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1017 | 26347329 |
US |
70 | 2 |
Injection site pain, Tendonitis, Plantar fasciitis, Low density lipoprotein increased, Gait disturbance, Device difficult to use, Drug dose omission by device, |
||||
EVOLOCUMAB, EVOLOCUMAB, |
||||
| 1018 | 26347419 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1019 | 26347423 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1020 | 26348238 |
US |
2 | |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1021 | 26350841 |
US |
||
Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1022 | 26350845 |
US |
||
Drug dose omission by device, Device delivery system issue, Device malfunction, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, UMECLIDINIUM, |
||||
| 1023 | 26338366 |
US |
1 | |
Drug dose omission by device, Device leakage, Accidental exposure to product, |
||||
SECUKINUMAB, FUROSEMIDE, AMLODIPINE, LISINOPRIL, |
||||
| 1024 | 26338455 |
US |
12 | 2 |
Anxiety, Fear of injection, Injection site pain, Wrong technique in product usage process, Device difficult to use, Drug dose omission by device, Device use issue, Device issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1025 | 26338472 |
US |
88 | |
Drug dose omission by device, Device delivery system issue, No adverse event, |
||||
DICLOFENAC SODIUM, DICLOFENAC SODIUM TOPICAL, DICLOFENAC SODIUM TOPICAL GEL, 1%, DICLOFENAC, DICLOFENAC SODIUM 1%, |
||||
| 1026 | 26338572 |
US |
63 | |
Panic reaction, Drug dose omission by device, Wrong technique in product usage process, Device deposit issue, Device delivery system issue, Off label use, |
||||
ALBUTEROL SULFATE, |
||||
| 1027 | 26338837 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1028 | 26339080 |
US |
||
Malaise, Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1029 | 26339081 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1030 | 26339088 |
US |
||
Drug dose omission by device, Device delivery system issue, Product quality issue, |
||||
TESTOSTERONE, TESTOSTERONE, |
||||
| 1031 | 26339250 |
US |
59 | 1 |
Chest pain, Wrong technique in product usage process, Device difficult to use, Drug dose omission by device, |
||||
EVOLOCUMAB, |
||||
| 1032 | 26339329 |
US |
36 | |
Product preparation error, Drug dose omission by device, Wrong technique in product usage process, No adverse event, |
||||
ALBUTEROL SULFATE, ALBUTEROL SULFATE, ALBUTEROL SULFATE, ALBUTEROL SULFATE, MONTELUKAST, CETIRIZINE HYDROCHLORIDE, |
||||
| 1033 | 26339445 |
US |
||
Asthma, Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, |
||||
| 1034 | 26339465 |
US |
70 | |
Drug dose omission by device, Wrong technique in product usage process, Device delivery system issue, No adverse event, |
||||
ALBUTEROL SULFATE, |
||||
| 1035 | 26340601 |
US |
14 | 1 |
Drug dose omission by device, Device delivery system issue, |
||||
FLUTICASONE PROPIONATE AND SALMETEROL, |
||||
| 1036 | 26341161 |
US |
1 | |
Accidental exposure to product, Device leakage, Drug dose omission by device, |
||||
SECUKINUMAB, |
||||
| 1037 | 26341448 |
KR |
7 | 2 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1038 | 26341450 |
US |
12 | 1 |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1039 | 26341451 |
CO |
2 | |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1040 | 26341452 |
US |
16 | 1 |
Drug dose omission by device, Device issue, |
||||
SOMATROPIN, |
||||
| 1041 | 26341453 |
GB |
7 | 2 |
Device defective, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1042 | 26341459 |
KR |
14 | 2 |
Drug dose omission by device, Device use error, Device mechanical issue, Device breakage, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1043 | 26342065 |
CO |
1 | |
Drug dose omission by device, Device leakage, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1044 | 26342108 |
US |
10 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1045 | 26342325 |
US |
14 | 1 |
Drug dose omission by device, Device information output issue, Device use issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1046 | 26342360 |
US |
72 | 1 |
Device malfunction, Device leakage, Accidental exposure to product, Drug dose omission by device, |
||||
SECUKINUMAB, |
||||
| 1047 | 26342416 |
US |
61 | 2 |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1048 | 26343558 |
US |
23 | 2 |
Injection site reaction, Injection site pain, Drug dose omission by device, |
||||
GALCANEZUMAB-GNLM, |
||||
| 1049 | 26343896 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1050 | 26332828 |
US |
2 | |
Device leakage, Accidental exposure to product, Needle issue, Drug dose omission by device, Device delivery system issue, |
||||
SECUKINUMAB, |
||||
| 1051 | 26332901 |
US |
||
Drug dose omission by device, Device issue, |
||||
FILGRASTIM-SNDZ, |
||||
| 1052 | 26333372 |
US |
||
Drug dose omission by device, Device breakage, Product packaging quantity issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, |
||||
| 1053 | 26333578 |
US |
1 | |
Device delivery system issue, Needle issue, Drug dose omission by device, |
||||
SUMATRIPTAN SUCCINATE, |
||||
| 1054 | 26333594 |
US |
||
Drug dose omission by device, Device delivery system issue, Device malfunction, Product packaging quantity issue, Expired product administered, Wrong technique in product usage process, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1055 | 26333595 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1056 | 26333834 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1057 | 26334097 |
US |
||
Drug dose omission by device, Device delivery system issue, Device malfunction, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1058 | 26334195 |
US |
||
Drug dose omission by device, Device delivery system issue, Product residue present, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1059 | 26334241 |
US |
||
Drug dose omission by device, Wrong technique in product usage process, Device malfunction, No adverse event, |
||||
ALBUTEROL SULFATE, |
||||
| 1060 | 26334698 |
US |
57 | 2 |
Injection site pain, Drug dose omission by device, |
||||
TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, TERIPARATIDE, |
||||
| 1061 | 26335025 |
US |
62 | 2 |
Injection site haemorrhage, Injection site bruising, Device difficult to use, Drug dose omission by device, |
||||
EVOLOCUMAB, EVOLOCUMAB, |
||||
| 1062 | 26335495 |
US |
||
Dyspnoea, Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1063 | 26335546 |
GB |
12 | 1 |
Device information output issue, Device occlusion, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1064 | 26335771 |
KR |
5 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1065 | 26335772 |
AR |
11 | 2 |
Drug dose omission by device, Device mechanical issue, Device physical property issue, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1066 | 26335774 |
GB |
10 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1067 | 26335776 |
CO |
1 | |
Drug dose omission by device, Device physical property issue, |
||||
SOMATROPIN, |
||||
| 1068 | 26335781 |
KR |
5 | 2 |
Device use error, Device material issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1069 | 26335918 |
GB |
21 | 1 |
Drug dose omission by device, Device power source issue, |
||||
SOMATROPIN, |
||||
| 1070 | 26335925 |
CO |
2 | |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1071 | 26335928 |
KR |
7 | 1 |
Drug dose omission by device, Device use error, Device material issue, |
||||
SOMATROPIN, |
||||
| 1072 | 26335948 |
US |
3 | 2 |
Drug dose omission by device, Device leakage, Device mechanical issue, Liquid product physical issue, Device delivery system issue, Device malfunction, |
||||
SOMATROPIN, |
||||
| 1073 | 26335949 |
PR |
15 | 1 |
Drug dose omission by device, Device issue, Device use error, Device breakage, |
||||
SOMATROPIN, |
||||
| 1074 | 26335950 |
CO |
2 | |
Drug dose omission by device, Device mechanical issue, Device malfunction, Device issue, Device occlusion, |
||||
SOMATROPIN, |
||||
| 1075 | 26335955 |
US |
1 | |
Drug dose omission by device, Device breakage, |
||||
SOMATROPIN, |
||||
| 1076 | 26335956 |
CO |
1 | |
Device leakage, Device physical property issue, Product knowledge deficit, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1077 | 26335958 |
CO |
2 | |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1078 | 26336061 |
US |
2 | |
Drug dose omission by device, Device malfunction, |
||||
ALBUTEROL SULFATE, |
||||
| 1079 | 26336170 |
US |
61 | 2 |
Device defective, Device issue, Drug dose omission by device, |
||||
SOMATROPIN, SOMATROPIN, SOMATROPIN, |
||||
| 1080 | 26336341 |
KR |
10 | 2 |
Drug dose omission by device, Device breakage, Device material issue, Product prescribing error, |
||||
SOMATROPIN, |
||||
| 1081 | 26336343 |
US |
9 | 1 |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1082 | 26336349 |
AR |
13 | 1 |
Product dose omission in error, Drug dose omission by device, Device mechanical issue, Device issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1083 | 26336364 |
UY |
12 | 1 |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1084 | 26336441 |
US |
12 | 1 |
Drug dose omission by device, Device use error, Device mechanical issue, Device breakage, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1085 | 26336444 |
US |
13 | 1 |
Drug dose omission by device, Device issue, |
||||
SOMATROPIN, |
||||
| 1086 | 26336445 |
US |
13 | 1 |
Device information output issue, Device issue, Device leakage, Device delivery system issue, Incorrect dose administered by device, Drug dose omission by device, |
||||
SOMATROPIN, BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, MOMETASONE FUROATE, ALBUTEROL SULFATE, |
||||
| 1087 | 26336450 |
US |
15 | 1 |
Drug dose omission by device, Device information output issue, Device power source issue, Device delivery system issue, |
||||
SOMATROPIN, |
||||
| 1088 | 26336451 |
EU |
17 | 1 |
Drug dose omission by device, Device mechanical issue, Device breakage, |
||||
SOMATROPIN, |
||||
| 1089 | 26336461 |
AR |
||
Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
| 1090 | 26336465 |
US |
16 | 1 |
Product prescribing error, Drug dose omission by device, Device use error, |
||||
SOMATROPIN, SOMATROPIN, SOMATROPIN, |
||||
| 1091 | 26336467 |
US |
17 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1092 | 26336478 |
AR |
9 | 2 |
Drug dose omission by device, Device leakage, Device issue, Device mechanical issue, |
||||
SOMATROPIN, TRIPTORELIN, |
||||
| 1093 | 26336479 |
US |
12 | 1 |
Drug dose omission by device, Device leakage, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1094 | 26336480 |
KR |
8 | 1 |
Device use error, Device material issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1095 | 26336485 |
EU |
5 | 2 |
Product packaging quantity issue, Device mechanical issue, Drug dose omission by device, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1096 | 26336494 |
AR |
||
Device defective, Drug dose omission by device, |
||||
ETANERCEPT, |
||||
| 1097 | 26336496 |
AR |
||
Device defective, Drug dose omission by device, |
||||
ETANERCEPT, |
||||
| 1098 | 26330298 |
US |
53 | 2 |
Psoriasis, Drug dose omission by device, Device difficult to use, |
||||
ETANERCEPT, ETANERCEPT, |
||||
| 1099 | 26330512 |
US |
20 | 2 |
Drug dose omission by device, Device difficult to use, Cough, |
||||
ERENUMAB-AOOE, ERENUMAB-AOOE, |
||||
| 1100 | 26330588 |
US |
80 | 2 |
Nasopharyngitis, Drug dose omission by device, |
||||
TERIPARATIDE, TERIPARATIDE, |
||||
disclaimer
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
2026-04-28