Drug:
Reaction: DRUG DOSE OMISSION BY DEVICE
20260101 - 20261231
No. 1201 - 1300
| No. | safetyreportid |
occurcountry |
patientonsetage |
patientsex 1:M 2:F |
|---|---|---|---|---|
Adverse reaction |
||||
Drug (openfda.generic_name, medicinalproduct) |
||||
| 1201 | 26315701 |
AR |
87 | 2 |
Device mechanical issue, Device failure, Device delivery system issue, Drug dose omission by device, Off label use, |
||||
ETANERCEPT, ETANERCEPT, |
||||
| 1202 | 26315726 |
US |
17 | 2 |
Drug dose omission by device, Device issue, |
||||
SOMATROPIN, |
||||
| 1203 | 26315728 |
GB |
60 | 2 |
Device power source issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1204 | 26315932 |
US |
||
Near death experience, Drug dose omission by device, Product quality issue, Device dispensing error, Device occlusion, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, DUPILUMAB, BIMATOPROST, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE, DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE SULFATE AND AMPHETAMINE ASPARTATE, SODIUM CHLORIDE, PREDNISONE, |
||||
| 1205 | 26316331 |
US |
2 | |
Condition aggravated, Device malfunction, Device deployment issue, Drug dose omission by device, |
||||
SECUKINUMAB, SECUKINUMAB, |
||||
| 1206 | 26316593 |
US |
65 | 1 |
Blood glucose increased, Drug dose omission by device, Device issue, Wrong technique in device usage process, Product storage error, Inappropriate schedule of product administration, |
||||
INSULIN GLARGINE, |
||||
| 1207 | 26316865 |
KR |
10 | 2 |
Drug dose omission by device, Device leakage, Device breakage, Liquid product physical issue, |
||||
SOMATROPIN, |
||||
| 1208 | 26317072 |
EU |
14 | 1 |
Device issue, Device mechanical issue, Drug dose omission by device, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1209 | 26317077 |
EU |
66 | 2 |
Device leakage, Device malfunction, Product knowledge deficit, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1210 | 26317079 |
EU |
10 | 1 |
Drug dose omission by device, Device mechanical issue, Device breakage, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1211 | 26317083 |
US |
9 | 2 |
Drug dose omission by device, Liquid product physical issue, |
||||
SOMATROPIN, SOMATROPIN, SOMATROPIN, SOMATROPIN, |
||||
| 1212 | 26317084 |
TR |
||
Drug dose omission by device, Device mechanical issue, Device leakage, |
||||
ETANERCEPT, |
||||
| 1213 | 26317772 |
KR |
10 | 2 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1214 | 26318242 |
US |
26 | 1 |
Drug dose omission by device, Device information output issue, Product prescribing error, |
||||
SOMATROPIN, |
||||
| 1215 | 26318289 |
CO |
1 | |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1216 | 26318524 |
US |
20 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1217 | 26318532 |
AR |
||
Drug dose omission by device, Device defective, |
||||
ETANERCEPT, |
||||
| 1218 | 26308141 |
US |
||
Dyspnoea, Drug dose omission by device, Off label use, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1219 | 26308144 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1220 | 26308148 |
US |
||
Drug dose omission by device, Device delivery system issue, Off label use, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1221 | 26308484 |
US |
18 | 2 |
Dermatitis atopic, Drug dose omission by device, Incorrect dose administered, |
||||
DUPILUMAB, |
||||
| 1222 | 26308568 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1223 | 26308573 |
US |
||
Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1224 | 26309056 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, LOSARTAN, FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE, |
||||
| 1225 | 26309643 |
US |
60 | |
Dyspnoea, Wheezing, Drug dose omission by device, Wrong technique in product usage process, Device delivery system issue, |
||||
ALBUTEROL SULFATE, |
||||
| 1226 | 26309893 |
CO |
2 | |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1227 | 26309909 |
US |
6 | 1 |
Drug dose omission by device, Device information output issue, Device physical property issue, Device delivery system issue, Device breakage, |
||||
SOMATROPIN, |
||||
| 1228 | 26310267 |
US |
68 | |
Drug dose omission by device, Device delivery system issue, No adverse event, |
||||
LEVALBUTEROL TARTRATE, |
||||
| 1229 | 26310308 |
US |
18 | 1 |
Drug dose omission by device, Device breakage, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1230 | 26310317 |
AR |
13 | 1 |
Device information output issue, Drug dose omission by device, Device use issue, |
||||
SOMATROPIN, |
||||
| 1231 | 26310345 |
US |
18 | |
Drug dose omission by device, Device delivery system issue, No adverse event, |
||||
LEVALBUTEROL TARTRATE, |
||||
| 1232 | 26310369 |
CO |
1 | |
Device information output issue, Device mechanical issue, Drug dose omission by device, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1233 | 26310372 |
US |
12 | 1 |
Drug dose omission by device, Device mechanical issue, Intentional product use issue, |
||||
SOMATROPIN, |
||||
| 1234 | 26310378 |
PR |
15 | 1 |
Drug dose omission by device, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1235 | 26310484 |
US |
74 | 2 |
Drug dose omission by device, Device delivery system issue, Device malfunction, Device mechanical issue, |
||||
BUDESONIDE AND FORMOTEROL FUMARATE, |
||||
| 1236 | 26310839 |
US |
||
Drug dose omission by device, Device malfunction, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1237 | 26311562 |
GB |
1 | 2 |
Product communication issue, Device use issue, Device issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1238 | 26311564 |
CO |
1 | |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1239 | 26311566 |
UY |
15 | 1 |
Device physical property issue, Device mechanical issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1240 | 26312024 |
US |
||
Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE, |
||||
| 1241 | 26312025 |
US |
||
Illness, Dyspnoea, Drug dose omission by device, Device delivery system issue, Product substitution issue, Off label use, Device mechanical issue, Product container seal issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1242 | 26312065 |
US |
57 | 2 |
Injection site pain, Injection site haemorrhage, Injection site erythema, Drug dose omission by device, |
||||
GALCANEZUMAB-GNLM, GALCANEZUMAB-GNLM, GALCANEZUMAB-GNLM, GALCANEZUMAB-GNLM, NIRMATRELVIR AND RITONAVIR, |
||||
| 1243 | 26312270 |
US |
||
Illness, Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, DROSPIRENONE AND ETHINYL ESTRADIOL, |
||||
| 1244 | 26304969 |
US |
2 | |
Myalgia, Drug dose omission by device, |
||||
ETANERCEPT, ETANERCEPT, ETANERCEPT, |
||||
| 1245 | 26305839 |
GB |
17 | 1 |
Device power source issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1246 | 26305842 |
US |
12 | 1 |
Drug dose omission by device, Device issue, Device connection issue, |
||||
SOMATROPIN, |
||||
| 1247 | 26305847 |
CO |
1 | |
Drug dose omission by device, Device information output issue, Device deployment issue, |
||||
SOMATROPIN, |
||||
| 1248 | 26305864 |
US |
1 | |
Drug dose omission by device, Device difficult to use, Device electrical finding, |
||||
SOMATROPIN, |
||||
| 1249 | 26305865 |
US |
15 | 2 |
Drug dose omission by device, Device use error, Device breakage, Device mechanical issue, |
||||
SOMATROPIN, |
||||
| 1250 | 26305895 |
KR |
6 | 2 |
Device material issue, Device use error, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1251 | 26305899 |
GB |
34 | 1 |
Drug dose omission by device, Device information output issue, Device breakage, |
||||
SOMATROPIN, |
||||
| 1252 | 26305901 |
CO |
13 | 1 |
Drug dose omission by device, Device defective, Product prescribing error, Off label use, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1253 | 26305922 |
CO |
2 | |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1254 | 26305939 |
US |
7 | 2 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1255 | 26305941 |
CO |
2 | |
Device leakage, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1256 | 26305943 |
US |
16 | 2 |
Drug dose omission by device, Device power source issue, |
||||
SOMATROPIN, |
||||
| 1257 | 26305946 |
PA |
13 | 1 |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1258 | 26305947 |
GB |
11 | 2 |
Drug dose omission by device, Device defective, |
||||
SOMATROPIN, |
||||
| 1259 | 26305962 |
CO |
1 | |
Drug dose omission by device, Device mechanical issue, Device breakage, Device defective, |
||||
SOMATROPIN, |
||||
| 1260 | 26305978 |
CO |
10 | 2 |
Device information output issue, Drug dose omission by device, Off label use, Off label use, |
||||
SOMATROPIN, |
||||
| 1261 | 26306411 |
US |
83 | 2 |
Device adhesion issue, Drug dose omission by device, |
||||
PEGFILGRASTIM, PEGFILGRASTIM, |
||||
| 1262 | 26303896 |
US |
82 | |
Drug dose omission by device, Device delivery system issue, Off label use, |
||||
LEVALBUTEROL TARTRATE, LISINOPRIL, |
||||
| 1263 | 26303922 |
US |
2 | |
Drug dose omission by device, Incorrect dose administered by device, Wrong technique in device usage process, Device leakage, |
||||
BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, |
||||
| 1264 | 26303965 |
US |
1 | |
Drug dose omission by device, Product packaging quantity issue, Product packaging issue, No adverse event, |
||||
DIAZEPAM, DIAZEPAM ORAL, DIAZEPAM ORAL SOLUTION (CONCENTRATE), |
||||
| 1265 | 26301765 |
CA |
||
Coronary artery thrombosis, Device leakage, Drug dose omission by device, |
||||
HEPARIN SODIUM, |
||||
| 1266 | 26301887 |
CO |
1 | |
Device information output issue, Drug dose omission by device, |
||||
SOMATROPIN, |
||||
| 1267 | 26301975 |
US |
18 | 1 |
Drug dose omission by device, Device power source issue, |
||||
SOMATROPIN, |
||||
| 1268 | 26302115 |
US |
14 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1269 | 26302997 |
US |
62 | 2 |
Exposure via skin contact, Device difficult to use, Accidental exposure to product, Drug dose omission by device, |
||||
ERENUMAB-AOOE, ERENUMAB-AOOE, |
||||
| 1270 | 26303338 |
US |
72 | 2 |
Inflammation, Odynophagia, Dysphagia, Drug dose omission by device, Accidental exposure to product, Exposure via skin contact, |
||||
DUPILUMAB, |
||||
| 1271 | 26303525 |
US |
66 | |
Chest discomfort, Dyspnoea, Drug dose omission by device, Device delivery system issue, Off label use, |
||||
ALBUTEROL SULFATE, ALBUTEROL SULFATE, |
||||
| 1272 | 26298437 |
US |
88 | 2 |
Drug ineffective, Chronic obstructive pulmonary disease, Device use issue, Device delivery system issue, Extra dose administered, Drug dose omission by device, Incorrect dose administered by device, Device malfunction, Speech disorder, Visual impairment, Ocular discomfort, |
||||
BUDESONIDE, GLYCOPYRROLATE, AND FORMOTEROL FUMARATE, BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, |
||||
| 1273 | 26299000 |
US |
56 | 2 |
Device difficult to use, Drug dose omission by device, Device use error, Headache, |
||||
ERENUMAB-AOOE, |
||||
| 1274 | 26299063 |
US |
||
Renal cancer, Drug dose omission by device, Device delivery system issue, Product packaging quantity issue, Wrong technique in product usage process, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, METFORMIN, METFORMIN ER 500 MG, METFORMIN ER 750 MG, LISINOPRIL, |
||||
| 1275 | 26299664 |
US |
||
Drug dose omission by device, Device delivery system issue, Device mechanical issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1276 | 26300375 |
US |
47 | 1 |
Accidental exposure to product, Drug dose omission by device, Device malfunction, Device leakage, |
||||
SECUKINUMAB, |
||||
| 1277 | 26301475 |
US |
2 | |
Drug dose omission by device, Device delivery system issue, |
||||
ADALIMUMAB, ADALIMUMAB-AATY, ADALIMUMAB-ADAZ, ADALIMUMAB-FKJP, ADALIMUMAB, ADALIMUMAB-AATY, ADALIMUMAB-ADAZ, ADALIMUMAB-FKJP, |
||||
| 1278 | 26292717 |
US |
82 | 2 |
Headache, Drug dose omission by device, |
||||
GALCANEZUMAB-GNLM, GALCANEZUMAB-GNLM, |
||||
| 1279 | 26292743 |
US |
63 | 2 |
Fear of injection, Injection site pain, Product storage error, Multiple use of single-use product, Device difficult to use, Drug dose omission by device, |
||||
EVOLOCUMAB, EVOLOCUMAB, |
||||
| 1280 | 26292766 |
US |
2 | |
Drug dose omission by device, Device adhesion issue, |
||||
ESTRADIOL, ESTRADIOL GEL 0.1%, ESTRADIOL TRANSDERMAL, ESTRADIOL,, |
||||
| 1281 | 26293037 |
US |
2 | |
Drug dose omission by device, Device malfunction, |
||||
GLATIRAMER ACETATE, GLATIRAMER ACETATE, |
||||
| 1282 | 26293098 |
US |
1 | |
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, |
||||
| 1283 | 26293235 |
US |
69 | 2 |
Device difficult to use, Wrong technique in product usage process, Injury associated with device, Accidental exposure to product, Drug dose omission by device, Incorrect disposal of product, Contusion, |
||||
EVOLOCUMAB, |
||||
| 1284 | 26293370 |
US |
50 | 2 |
Drug dose omission by device, Device malfunction, |
||||
ADALIMUMAB-ADAZ, ADALIMUMAB-ADAZ, |
||||
| 1285 | 26293481 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1286 | 26294009 |
US |
2 | |
Asthma, Product storage error, Drug ineffective, Drug dose omission by device, Dyspnoea, Device use issue, Device delivery system issue, Incorrect dose administered, |
||||
BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE, |
||||
| 1287 | 26294489 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1288 | 26294493 |
US |
||
Off label use, Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, LORATADINE, LORATADINE ORAL, |
||||
| 1289 | 26294823 |
US |
||
Drug dose omission by device, Off label use, Product quality issue, Device malfunction, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1290 | 26294920 |
US |
||
Off label use, Drug dose omission by device, Device delivery system issue, Device malfunction, Device mechanical issue, Malaise, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, CEFUROXIME AXETIL, AZITHROMYCIN, AZITHROMYCIN MONOHYDRATE, AZITHROMYCIN DIHYDRATE, |
||||
| 1291 | 26294921 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, SERTRALINE, SERTRALINE, PERPHENAZINE, GABAPENTIN, |
||||
| 1292 | 26295085 |
US |
||
Drug dose omission by device, Device delivery system issue, |
||||
ALBUTEROL SULFATE, ALBUTEROL, ALBUTEROL SULFATE, ALBUTEROL, |
||||
| 1293 | 26296327 |
US |
11 | 1 |
Injection site discharge, Drug dose omission by device, Wrong technique in device usage process, |
||||
SOMATROPIN, |
||||
| 1294 | 26296397 |
US |
13 | 1 |
Drug dose omission by device, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1295 | 26296502 |
US |
9 | 1 |
Drug dose omission by device, Device mechanical issue, Device leakage, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1296 | 26296503 |
PA |
13 | 1 |
Drug dose omission by device, Device delivery system issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1297 | 26296508 |
AR |
9 | 2 |
Drug dose omission by device, Device mechanical issue, Device information output issue, |
||||
SOMATROPIN, |
||||
| 1298 | 26296509 |
US |
14 | 1 |
Drug dose omission by device, Device breakage, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1299 | 26296510 |
CO |
2 | |
Device mechanical issue, Device information output issue, Injection site pain, Stress, Device difficult to use, Drug dose omission by device, |
||||
SOMATROPIN, SOMATROPIN, |
||||
| 1300 | 26296512 |
US |
74 | 2 |
Drug dose omission by device, Product communication issue, Device delivery system issue, |
||||
SOMATROPIN, SOMATROPIN, |
||||
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