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side effects patient, weighting 196.2 lb, was diagnosed with delirium tremens, hypertension and took Haldol-janssen Patient was hospitalized.. View more Serious Adverse Events reported to FDA.

List of Haldol-janssen Adverse Effects reported to US Food and Drug Administration (FDA)

Hypokalaemia, Long Qt Syndrome, Torsade De Pointes (6523764-X)
on Dec 30, 2009 Male patient from GERMANY , weighting 196.2 lb, was diagnosed with
  • delirium tremens
and was treated with Haldol-janssen. Patient experienced the following unwanted or unexpected effects: hypokalaemia, long qt syndrome, torsade de pointes. Haldol-janssen dosage: N/A. Patient was hospitalized.

Convulsion, Overdose, Suicide Attempt, Vomiting (4803407-3)
Patient was taking Haldol-janssen Forte 10 Mg. Patient had the following side effects: convulsion, overdose, suicide attempt, vomiting on Oct 11, 2005 from GERMANY Additional patient health information: Female patient , weighting 132.3 lb, . Haldol-janssen Forte 10 Mg dosage: N/A.

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Side Effects reported to FDA: 2. View FDA Adverse Reports

Haldol-janssen safety alerts: No

Reported hospitalizations: 1

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Haldol-janssen Adverse Reactions

Convulsion ( 1 Reports)

Hypokalaemia ( 1 Reports)

Long Qt Syndrome ( 1 Reports)

Overdose ( 1 Reports)

Suicide Attempt ( 1 Reports)

Torsade De Pointes ( 1 Reports)

Vomiting ( 1 Reports)

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