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

TOOTH MALFORMATION ( 5 FDA reports)
TOOTH DISORDER ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MECONIUM STAIN ( 5 FDA reports)
HYPERMETROPIA ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CRANIOSYNOSTOSIS ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
CLEFT PALATE ( 3 FDA reports)
NAUSEA ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POISONING ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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