MedsFacts Reports covering ADVIL ENFANTS ET NOURRISSONS
Directory listing ordered by most common adverse events for ADVIL ENFANTS ET NOURRISSONS
Please choose an event type to view the corresponding MedsFacts report:
CELLULITIS ( 10 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
BLISTER ( 4 FDA reports)
RASH MACULAR ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PAIN ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
URTICARIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
MASS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
BLISTER ( 4 FDA reports)
RASH MACULAR ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PAIN ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
URTICARIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
MASS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)