MID-VOLUME · DEATH-HEAVY

ranibizumab Side Effects

ranibizumab (also sold as Lucentis) sits MID-VOLUME #206 of 524 by FAERS report count. Lead signal: DEATH-HEAVY - 19.4% of FAERS reports list death as an outcome (5,072 of 26,174). Demographics and serious-outcome tables follow.

Data updated 2026-05-15

26,174
FAERS reports

FDA Adverse Event Reporting System extract for ranibizumab. Stamp set CASELOAD · DEATH-HEAVY · HOSP-MID. How figures are compiled.

ranibizumab: 19.4% of FAERS reports list death as an outcome (5,072 of 26,174). Caseload stamp CASELOAD; volume band MID-VOLUME #206 of 524 by FAERS report count.

Mid-book FAERS page for ranibizumab (Lucentis) (26,174 reports). Signature DEATH-HEAVY. Dominant age band on file: 75+. Educational reference only.

Counts from the openFDA FAERS extract (2005–2025). Stamps CASELOAD · DEATH-HEAVY · HOSP-MID · SEX-BALANCED.

DEATH leads 3,783 of 26,174 reports

DEATH
3,783
VISUAL ACUITY REDUCED
2,888
VISUAL IMPAIRMENT
1,623
CEREBROVASCULAR ACCIDENT
1,235
EYE HAEMORRHAGE
1,041
BLINDNESS
1,036
VISION BLURRED
1,029
EYE PAIN
954
RETINAL HAEMORRHAGE
789
ENDOPHTHALMITIS
727
MYOCARDIAL INFARCTION
688
CATARACT
681
VITREOUS FLOATERS
618
FALL
590
MALAISE
582
MACULAR OEDEMA
574
HEADACHE
484

Who reports · age peak 75+ (SEX-BALANCED)

Sex coding · SEX-BALANCED

Female 12,771 (56%)
Male 9,954 (43%)
Unknown 210

Age peak 75+ (6,674 reports)

0-17 75 (1%)
18-44 442 (4%)
45-64 2,417 (19%)
65-74 2,945 (23%)
75+ 6,674 (53%)

FAERS filings rising toward 2025

2005 2025

Reactions in Death Reports

Death-mentioned subset is HEAVY here (5,072 reports, 19.4%). Top co-reported reactions in that subset - voluntary, not causal.

Reaction Reports
DEATH 3,778
MYOCARDIAL INFARCTION 203
CEREBROVASCULAR ACCIDENT 172
PNEUMONIA 106
VISUAL ACUITY REDUCED 81
FALL 77
CARDIAC FAILURE 69
CARDIAC ARREST 67
MYOCARDIAL ISCHAEMIA 64
ATRIAL FIBRILLATION 57
CARDIAC FAILURE CONGESTIVE 57
MALAISE 54
HYPERTENSION 49
NEOPLASM MALIGNANT 42
SEPSIS 38
RENAL FAILURE 36
BRONCHOPNEUMONIA 35
GENERAL PHYSICAL HEALTH DETERIORATION 33
LUNG NEOPLASM MALIGNANT 32

Reactions in Hospitalization Reports

Hospitalization mid-share (4,781, 18.3%). Co-reported reactions:

Reaction Reports
CEREBROVASCULAR ACCIDENT 567
VISUAL ACUITY REDUCED 398
FALL 337
MYOCARDIAL INFARCTION 319
PNEUMONIA 243
MALAISE 198
VISUAL IMPAIRMENT 198
CEREBRAL INFARCTION 192
VISION BLURRED 166
ENDOPHTHALMITIS 158
EYE PAIN 154
TRANSIENT ISCHAEMIC ATTACK 143
HYPERTENSION 142
ATRIAL FIBRILLATION 133
DYSPNOEA 133
EYE HAEMORRHAGE 127
RETINAL HAEMORRHAGE 125
DEATH 113
BLINDNESS 110
How to read ranibizumab FAERS figures (CASELOAD · DEATH-HEAVY · HOSP-MID)

FAERS holds 26,174 voluntary reports linked to ranibizumab (Lucentis), 2005-2025. Death is listed on 5,072 (19.4%). Hospitalization appears on 4,781 (18.3%). Top co-reported indication: Product Used For Unknown Indication.

Mid-volume extract - treat DEATH-HEAVY · HOSP-MID as signal-detection rates next to 19.4% of FAERS reports list death as an outcome (5,072 of 26,174).

Read with ranibizumab

Peers ranked by ABS(total_reports), then an ABS(death_share) pole; guide hop follows DEATH-HEAVY · HOSP-MID stamps.