Please choose an event type to view the corresponding MedsFacts report:

PAIN ( 12 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
OVARIAN CYST ( 7 FDA reports)
COUGH ( 7 FDA reports)
ORAL HERPES ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
TRANSFUSION ( 4 FDA reports)
FRACTURE NONUNION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
RICKETS ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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