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REPORTED SIGNALS

somatropin

Genotropin · Humatrope · Norditropin

Registration status unknownDrughormonesNovo Nordisk
SUBCUTANEOUS

1 INDICATIONS AND USAGE NORDITROPIN is a recombinant human growth hormone indicated for: • Pediatric : Treatment of pediatric patients with growth failure due to inadequate secretion of endogenous growth hormone (GH), short stature associated with Noonan syndrome, short stature associated with Turner syndrome, short stature born small for gestational age (SGA) with no catch-up growth by age 2 to 4 years, Idiopathic Short Stature (ISS), and growth failure due to Prader-Willi Syndrome ( 1.1 ) • Adult : Replacement of endogenous GH in adults with growth hormone deficiency ( 1.2 ) 1.1 Pediatric Patients NORDITROPIN is indicated for the treatment of pediatric patients with: • growth failure due to inadequate secretion of endogenous growth hormone (GH), • short stature associated with Noonan syndrome, • short stature associated with Turner syndrome, • short stature born small for gestational age (SGA) with no catch-up growth by age 2 years to 4 years of age, • Idiopathic Short Stature (ISS), height standard deviation score (SDS) <-2.25, and associated with growth rates unlikely to permit attainment of adult height in the normal range, • growth failure due to Prader-Willi syndrome (PWS). 1.2 Adult Patients NORDITROPIN is indicated for the replacement of endogenous GH in adults with growth hormone deficiency (GHD)

Mechanism. 12.1 Mechanism of Action Somatropin binds to dimeric GH receptors located within the cell membranes of target tissue cells. This interaction results in intracellular signal transduction and subsequent induction of transcription and translation of GH-dependent proteins including IGF-1, IGF BP-3 and acid-labile subunit. Somatropin has direct tissue and metabolic effects or mediated indirectly by IGF-1, including stimulation of chondrocyte differentiation, and proliferation, stimulation hepatic glucose output, protein synthesis and lipolysis. Somatropin stimulates skeletal growth in pediatric patients with GHD as a result of effects on the growth plates (epiphyses) of long bones. The stimulation of skeletal growth increases linear growth rate (height velocity) in most somatropin-treated pediatric patients. Linear growth is facilitated in part by increased cellular protein synthesis.

71.462
reports (FAERS)
26.0%
reported as serious
986
fatal reports (1.4%)
30
signals above threshold
1986
first approved
2026-07
last updated
TIMELINE · FDA MILESTONES
Approved
1986
Class II recall
2016
1985
2026
SIGNAL RANKING · ROR

Wat opvalt in de meldingen.

In bijsluiterNieuw signaalOnbekend & frequent
Symptoom
0.1110100
ROR [95% CI]
Device Information Output Issue
2838.9 [2618.63077.7]
Device Mechanical Issue
509.1 [490.1528.9]
Device Power Source Issue
343.3 [318.1370.4]
Expired Device USED
243.9 [227.3261.7]
Device Physical Property Issue
185.8 [177.1195.0]
POOR Quality Device USED
175.0 [167.4183.0]
Device Material Issue
146.1 [132.7160.9]
Circumstance OR Information Capable OF Leading TO Device USE Error
141.7 [129.8154.6]
DRUG DOSE Omission BY Device
117.1 [114.9119.3]
Device Leakage
112.3 [109.7115.0]
Device Breakage
101.8 [99.3104.3]
Device USE Issue
57.3 [55.059.7]
Device Defective
46.6 [44.448.8]
Wrong Technique IN Device Usage Process
38.1 [36.939.3]
Incorrect DOSE Administered BY Device
37.7 [36.239.3]

ROR = reporting odds ratio (log-schaal). Een waarde boven 1 betekent dat het symptoom vaker wordt gemeld voor dit product dan voor alle andere producten samen. Dit meet hoeveel het opvalt in meldingen — geen causaliteit, geen risico.

INTERPRETATION
Auto-gegenereerd

Bij somatropine worden vaak meldingen gedaan over problemen met het injectieapparaat, zoals moeilijk gebruik of defecten. Dit is logisch, omdat somatropine vaak via een injectiepen wordt toegediend. Ook bloeduitstortingen en bloedingen op de injectieplaats worden relatief vaak gemeld. Dit kan komen door de injectie zelf. "Vaak gemeld" is niet hetzelfde als "vaak veroorzaakt". Dit vervangt geen medisch advies.

Dit vervangt geen medisch advies.

LABEL VERSUS REPORT
On the label

No signals currently mapped to the label.

Newly reported
Device Information Output Issue
Device Mechanical Issue
Device Power Source Issue
Expired Device USED
Device Physical Property Issue
POOR Quality Device USED
Device Material Issue
Circumstance OR Information Capable OF Leading TO Device USE Error
REPORTS OVER TIME

Report volume per quarter.

19861987198819891991
RECALL HISTORY · 1 ON RECORD
DateClassReasonFirm
Apr 27, 2016IIDefective Delivery System; may have a low frequency assembly fault which may result in pens block during the so-called "air shot" stepNovo Nordisk Inc

Class I = reasonable probability of serious harm · Class II = temporary or reversible · Class III = unlikely to cause harm. Source: openFDA enforcement.

BRON & CITATIE
HealthProves. somatropin — reported signals. Retrieved 2026-07-04. Source: openFDA (FAERS). healthproves.com/somatropin/
FAERS71,462 records
Opgehaald2026-07-04
MethodeROR / disproportionaliteit