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Abilify and Nausea

This page shows results related to Abilify and Nausea from the FDA Adverse Event Reporting System (AERS).

Click here to learn about all Abilify adverse events.

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Abilify and Nausea

Age

20-29 Years
61
30-39 Years
55
10-19 Years
53
40-49 Years
52
>60 Years
44
50-59 Years
38
1-9 Years
10
0-12 Months
1

Gender

Male: 31%
Female: 59%
Gender Unknown: 10%

Outcome

What were the most common outcomes of those reporting Nausea?

Other
121
Hospitalization
82
Death
14
Life Threatening
11
Disability
8
Required Intervention
3

Reporter

Who most commonly reported Nausea?

Consumer
211
Physician
90
Other
88
Pharmacist
16
Lawyer
1

Therapy

Of those reporting Nausea, why were they taking Abilify?

Bipolar Disorder
84
Depression
39
Schizophrenia
37
Psychotic Disorder
20
Anxiety
16

Other Medications

Which medications reported to the FDA are most commonly associated with Nausea?

Byetta
13836
Chantix
13125
Humira
5307
Forteo
4638
Fosamax
4052
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Enbrel
4039
Yaz
3605
Vioxx
3562
Tysabri
3043
Yasmin
2927
Remicade
2799
Victoza
2731
Zometa
2591
Cymbalta
2575
Digoxin
2199
Lyrica
2150
Cisplatin
2111
Paxil
2033
Heparin Sodium Injection
1967
Sandostatin Lar
1924
Aredia
1725
Gleevec
1704
Avonex
1682
Mirena
1676
Exjade
1635
Pristiq
1542
Carboplatin
1461
Oxycontin
1435
Seroquel
1398
Nexium
1357
Pegasys
1352
Ortho Evra
1335
Duragesic-100
1313
Ribavirin
1312
Accutane
1311
Fluorouracil
1307
Niaspan
1300
Plan B One-step
1289
Peg-intron
1203
Nexavar
1163
Rebif
1140
Effexor Xr
1082
Sutent
1048
Cyclophosphamide
1018
Avastin
1016
Crestor
1006
Gilenya
1002
Strattera
994
Capecitabine
983
Revlimid
975
Oxaliplatin
974

Is the adverse drug reaction you’re experiencing actually due to the drug you took?

The Naranjo Scale is a questionnaire for determining the likelihood of whether an adverse drug reaction is actually due to the drug or caused by other factors. Probability is assigned via a score termed definite, probable, possible or doubtful.*

YESNOUNKOWN
Are there previous conclusive reports on this reaction?
Did the adverse event appear after the suspected drug was administered?
Did the adverse reaction improve when the drug was discontinued or a specific antagonist was administered?
Did the adverse reaction reappear when the drug was readministered?
Are there alternative causes (other than the drug) that could on their own have caused the reaction?
Did the reaction reappear when a placebo was given?
Was the drug detected in the blood (or other fluids) in concentrations known to be toxic?
Was the reaction more severe when the dose was increased, or less severe when the dose was decreased?
Did the patient have a similar reaction to the same or similar drugs in any previous exposure?
Was the adverse event confirmed by any objective evidence?
Probability of an Adverse Event
Doubtful
Possible
Probable
Definite

*Naranjo, et al. "A method for estimating the probability of adverse drug reactions." Clin Pharmacol Ther. 1981 Aug;30(2):239-45.

To learn more about all adverse events for Abilify, view the complete Abilify adverse event report.

Scientific Publications on Nausea

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